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

TOWEL CLIPS

K Number: K890159 · Decision Feb 3, 1989
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
13
Applicant Total
14
Review Days
25

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
TOWEL CLIPS
K Number
K890159
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dhason Brothers, Inc.
Date Received
January 9, 1989
Decision Date
February 3, 1989
Product Code
GDO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GDO Applier, Surgical, Clip

Similar 510(k) Clearances

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

View all

Other Clearances by Dhason Brothers, Inc.

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