Regulatory document
Tissue Mimicking Material (TMM) for Preclinical Acoustic Performance Characterization of…
FDA MDDT · Guidance · USA · Jul 10, 2019
Key facts
| Title | Tissue Mimicking Material (TMM) for Preclinical Acoustic Performance Characterization of High Intensity Therapeutic Ultrasound (HITU) Devices |
|---|---|
| Issuer | FDA Medical Device Development Tools |
| Source | FDA MDDT |
| Document type | Guidance |
| Country or region | USA |
| Date | Jul 10, 2019 |
| Document | fda.gov |
| Issuer website | fda.gov |
At a glance
- Yes Full text searchable in Orca1
- 10–99 Documents from this issuer in Orca1
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Global regulations and guidance
Regulations, guidance and official notices from medical device and medicines regulators worldwide, collected by Orca1 from each issuer's website. Only the title, issuer, date and link are shown here; the full text is searchable in Orca1.
Source: Medical device and medicines regulators and agencies as named on each record (EMA, MHRA, TGA, CDSCO, PMDA, NMPA, Health Canada, HSA, the FDA and others), collected by Orca1 from each issuer's website · Source date: