510(k) K802457
K802457 is an FDA 510(k) premarket notification submitted by J. Sklar Mfg. Co., Inc. for the device "KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610". The FDA issued a decision of Substantially Equivalent on January 12, 1981. The device falls under product code HFB (Forceps, Biopsy, Gynecological), a Class I device regulated under 21 CFR 884.4530. J. Sklar Mfg. Co., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 12, 1981
- Date Received
- October 8, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Forceps, Biopsy, Gynecological
- Device Class
- Class I
- Regulation Number
- 884.4530
- Review Panel
- OB
- Submission Type