ANAGO DISP., ALL PURPOSE PATIENT REST.— 510(k) K800197
Substantially EquivalentAnago, Inc.
FDA 510(k) clearance K800197 for ANAGO DISP., ALL PURPOSE PATIENT REST., Substantially Equivalent on 1980-02-26. Applicant: Anago, Inc.. Device class: 1.
Clearance details
- Applicant
- Anago, Inc.
- Product code
- Code FQM
- Device class
- Class 1
- Regulation
- 21 CFR 880.5075
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code FQM
view all- K040936 — PETIT SILMA ELASTIC BANDAGE WITH GERMANIUM/TITANIUM OXIDE
- K040054 — BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE
- K013244 — COMFORTCARE COMPRESSION SUPPORT WITIH MAGNETS AND AEGIS MICROBE SHIELD COMFORTCARE MAGNETIC INSOLES AND AEGIS MICROBE
- K952738 — SKIN SAVER SYSTEMS
- K872868 — ASPEN ESMARK BANDAGE
More clearances from Anago, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.