510(k) K851799

61-100 TO 61-124 VARIOUS VAGINAL SPECVIA(CUSCO,GRA by Artiberia — Product Code HDF

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