510(k) K851799
K851799 is an FDA 510(k) premarket notification submitted by Artiberia for the device "61-100 TO 61-124 VARIOUS VAGINAL SPECVIA(CUSCO,GRA". The FDA issued a decision of Substantially Equivalent on May 22, 1985. The device falls under product code HDF (Speculum, Vaginal, Metal), a Class I device regulated under 21 CFR 884.4520. Artiberia has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 22, 1985
- Date Received
- April 25, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Speculum, Vaginal, Metal
- Device Class
- Class I
- Regulation Number
- 884.4520
- Review Panel
- OB
- Submission Type