FDA device listing

PARA FLOCKED SWAB GB946DP,PARA FLOCKED SWAB GB946NP,PARA FLOCKED SWAB GB946OP,PARA POLYESTER SWAB GB946PS,PMW Flocked…

FDA device listing 1812528884 · PMWCORPORATION

Key facts

Proprietary names PARA FLOCKED SWAB GB946DP,PARA FLOCKED SWAB GB946NP,PARA FLOCKED SWAB GB946OP,PARA POLYESTER SWAB GB946PS,PMW Flocked Swab PMW-NS SWAB,PMW Flocked Swab PMW-SWAB DUAL,PMW Flocked Swab PMW-SWAB NP1,PMW Flocked Swab PMW-SWAB OP2,PMW Spun Swab PMW POLYESTER SPUN SWAB,PMW Spun Swab PMW RAYON SWAB,PMW-SWAB PMW CONTROL SWAB,RADI Flocked Swab OD103DB,RADI Flocked Swab OD103NB,RADI Flocked Swab…
Owner/operator PMWCORPORATION
Owner/operator number 10075535
Product codes FRL
Device names FRL - Fiber, Medical, Absorbent
Device class Class I
Classification regulations (21 CFR) 880.5300
Review panels General Hospital
Registered establishments PMWCORPORATION
Establishment registrations 3017252880
FEI numbers 3017252880
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings