FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

UTERINE MANIPULATORS

K Number: K812204 · Decision Oct 13, 1981
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
14
Applicant Total
9
Review Days
70

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
UTERINE MANIPULATORS
K Number
K812204
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.4520
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Reznik Instruments
Date Received
August 4, 1981
Decision Date
October 13, 1981
Product Code
KOH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KOH Instrument, Manual, General Obstetric-Gynecologic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KOH), ordered by most recent decision date.

View all

Other Clearances by Reznik Instruments

K Number Device Name
K812205 FORCEP
K812201 PHOTOGRAPHIC EQUIPMENT
K812203 ELECTROSURGICAL UNIT
K812206 LAPAROSCOPE
K812199 TROCAR & TROCAR SLEEVES
K812200 INSUFFLATOR
K812202 FIBER OPTIC LIGHT SOURCE
K812198 ACCESSORIES(PROBES, SUCTION TUBES, ETC.)