510(k) K802785
K802785 is an FDA 510(k) premarket notification submitted by Secol Co. for the device "ELASTIC BANDAGE". The FDA issued a decision of Substantially Equivalent on December 11, 1980. The device falls under product code FQM (Bandage, Elastic), a Class I device regulated under 21 CFR 880.5075. Secol Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 11, 1980
- Date Received
- November 4, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bandage, Elastic
- Device Class
- Class I
- Regulation Number
- 880.5075
- Review Panel
- HO
- Submission Type