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

FORCEPS

K Number: K890157 · Decision Feb 13, 1989
Classifications
1
FEI Numbers
1140
Registration Numbers
1140
Same Product Code
57
Applicant Total
14
Review Days
35

Basic Information

Device Name
FORCEPS
K Number
K890157
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
DHASON BROTHERS, INC.
Date Received
January 9, 1989
Decision Date
February 13, 1989
Product Code
LXH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
LXH Orthopedic Manual Surgical Instrument

Similar 510(k) Clearances

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

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Other Clearances by DHASON BROTHERS, INC.

K Number Device Name
K890158 RETRACTORS
K890168 RETRACTOR, SELF-RETAINING
K890160 GOUGES FOR FEMORAL HEADS
K890161 THOMPSON TYPE RASP W/TOMMY BAR
K890164 HUDSON BRACE W/BURRS
K890156 IMPACTOR FOR FEMORAL HEAD
K890166 RONGUER-ORTHOPEDIC
K890162 EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD
K890165 FORCEPS-ORTHOPEDIC
K890163 AUSTIN MOORE HALLOW CHISEL
Search all 14 clearances from DHASON BROTHERS, INC. →