510(k) K842112
K842112 is an FDA 510(k) premarket notification submitted by J. Sklar Mfg. Co., Inc. for the device "TISCHLER CERVICAL BIOPSY PUNCH FORCEPS". The FDA issued a decision of Substantially Equivalent on July 3, 1984. 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
- July 3, 1984
- Date Received
- May 29, 1984
- 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