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

OMS/GONVERS RETINAL PERFORATOR

K Number: K844448 · Decision Aug 21, 1985
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
1
Applicant Total
21
Review Days
278

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
OMS/GONVERS RETINAL PERFORATOR
K Number
K844448
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Optical Micro Systems, Inc.
Date Received
November 16, 1984
Decision Date
August 21, 1985
Product Code
HNM
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
HNM Needle, Ophthalmic Suturing

Similar 510(k) Clearances

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

View all

Other Clearances by Optical Micro Systems, Inc.

K Number Device Name
K950218 OMS SLIMLINE PHACO HANDPIECE
K946054 DIPLOMAX
K935223 OPHTHALMIC SURGICAL SYSTEM
K935226 I/V POLE
K935003 ELECTRIC I/V POLE OR EIVP2
K870068 ASPIRATION REVERSAL CONTROL (ARC) MODULE
K844373 O.M.S. ULTRA-PHACO
K844895 OMS SILICONE OIL INJECTOR
K844467 OMS CRYO
K844715 VISC-X VITREOUS ASPIRATING & CUTTING INSTRUMENT SY
Search all 21 clearances from Optical Micro Systems, Inc. →