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

FIX. & LENS FOR. #'S 3510,3512,3248,3795

K Number: K791986 · Decision Oct 4, 1979
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
43
Applicant Total
140
Review Days
9

Basic Information

Device Name
FIX. & LENS FOR. #'S 3510,3512,3248,3795
K Number
K791986
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
EDWARD WECK, INC.
Date Received
September 25, 1979
Decision Date
October 4, 1979
Product Code
HNR
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HNR Forceps, Ophthalmic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HNR), 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. →