FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

D.O.R.C. MICRODIATHERMY SYSTEM

K Number: K962135 · Decision Aug 29, 1996
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
11
Applicant Total
10
Review Days
87

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
D.O.R.C. MICRODIATHERMY SYSTEM
K Number
K962135
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4115
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dutch Ophthalmic USA, Inc.
Date Received
June 3, 1996
Decision Date
August 29, 1996
Product Code
HQO
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
HQO Unit, Cautery, Thermal, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Dutch Ophthalmic USA, Inc.

K Number Device Name
K012821 D.O.R.C. CRYOSTAR CRYOSURGICAL SYSTEM
K010082 D.O.R.C. HARMONY TOTAL TTC VITRECTOMY SYSTEM
K983797 D.O.R.C. HARMONY TOTAL VITRECTOMY SYSTEM
K980636 FIBER OPTIC ENDOILLUMINATION PROBE
K973229 D.O.R.C. HEXON ILLUMINATION SYSTEM
K973757 D.O.R.C. SOLUX LIGHT SOURCE
K954842 D.O.R.C. VFI/VFE SYSTEM
K940373 OPHTHALMIC CRYO UNIT
K902491 ECKHARDT TEMPORARY KERATOPROSTHESIS