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

OPHTHALMIC CRYO UNIT

K Number: K940373 · Decision Jul 18, 1994
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
10
Applicant Total
10
Review Days
173

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Basic Information

Device Name
OPHTHALMIC CRYO UNIT
K Number
K940373
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4170
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dutch Ophthalmic USA, Inc.
Date Received
January 26, 1994
Decision Date
July 18, 1994
Product Code
HPS
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
HPS Unit, Cryophthalmic

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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
K962135 D.O.R.C. MICRODIATHERMY SYSTEM
K954842 D.O.R.C. VFI/VFE SYSTEM
K902491 ECKHARDT TEMPORARY KERATOPROSTHESIS