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

FLOOR LINE INSTRUMENTS

K Number: K791741 · Decision Oct 4, 1979
Classifications
1
FEI Numbers
251
Registration Numbers
251
Same Product Code
51
Applicant Total
140
Review Days
24

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
FLOOR LINE INSTRUMENTS
K Number
K791741
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Edward Weck, Inc.
Date Received
September 10, 1979
Decision Date
October 4, 1979
Product Code
FZT
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
FZT Cutter, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Edward Weck, Inc.

K Number Device Name
K915378 WECK TROCAR
K914690 LM15(TM), CATALOG NUMBER - 523821
K911915 HEMOCLIP II
K914470 PNEUMO-SEAL(TM)
K911272 ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705
K902108 HEM-O-LOK(TM)
K902232 WECK ELECTROSURGICAL GENERATOR #174200
K897045 BOWIE-DICK TEST CARD CATALOG NUMBER 008018
K871110 CORONARY ARTERY BYPASS GRAFT (CABG) MARKER
K851251 AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200
Search all 140 clearances from Edward Weck, Inc. →