510(k) K801532
K801532 is an FDA 510(k) premarket notification submitted by The Owenby Co. for the device "STOCKINETTE, STERILE TWO PLY W/PULL TABS". The FDA issued a decision of Substantially Equivalent on July 28, 1980. The device falls under product code FQM (Bandage, Elastic), a Class I device regulated under 21 CFR 880.5075. The Owenby Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 28, 1980
- Date Received
- July 1, 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