510(k) K761192
K761192 is an FDA 510(k) premarket notification submitted by Superior Plastic Products Corp. for the device "DRESSING CHANGE KIT". The FDA issued a decision of Substantially Equivalent on February 28, 1977. The device falls under product code JOK (Scissors, Medical, Disposable), a Class I device regulated under 21 CFR 880.6820. Superior Plastic Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 28, 1977
- Date Received
- December 6, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Scissors, Medical, Disposable
- Device Class
- Class I
- Regulation Number
- 880.6820
- Review Panel
- HO
- Submission Type