FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MALLAWANY ATRAUMATIC TISSUE FORCEPS

K Number: K922248 · Decision Feb 17, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
5
Review Days
645

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
MALLAWANY ATRAUMATIC TISSUE FORCEPS
K Number
K922248
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Numed Technologies, Inc.
Date Received
May 13, 1992
Decision Date
February 17, 1994
Product Code
HET
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
HET Laparoscope, Gynecologic (And Accessories)

Similar 510(k) Clearances

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

View all

Other Clearances by Numed Technologies, Inc.

K Number Device Name
K930571 REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING
K931501 NUMED DISPOSABLE ATT. NUMED HANDLE LAP. INST.
K923126 MALLAWANY TISSUE GRASPING FORCEPS
K923055 OPERATING SCISSORS FOR LAPAROSCOPIC SURGERIES