Medical Device Manufacturer · US , Walker , MI

United Surgical Corp.

7 submissions · 7 cleared · Since 1983

Total

Cleared

Denied

United Surgical Corp. — FDA 510(k) Submissions

United Surgical Corp. has submitted 7 FDA 510(k) premarket notifications since 1983, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Phacofragmentation, Unit, Cryophthalmic, Stapler, Surgical, Instrument, Vitreous Aspiration And Cutting, Ac-powered, Apparatus, Cautery, Radiofrequency, Ac-powered . Use the specialty filter in the sidebar to narrow results.

7 devices

1–7 of 7

PIEZO HANDPIECE

K902150 · HQC Unit, Phacofragmentation · Ophthalmic

Jul 1990 51d

PHACOTRON DAY PAK

K870671 · HQC Unit, Phacofragmentation · Ophthalmic

Apr 1987 46d

NON-STERILE, EXTRA PLUS PAK CAT. #USPK 2100

K870806 · HQC Unit, Phacofragmentation · Ophthalmic

Mar 1987 28d

UNITED SURGICAL CORP. DIATHERMIC PLUS

K870194 · HQR Apparatus, Cautery,... · Ophthalmic

Feb 1987 31d

UNITED SURGICAL CORP. CRYOPTIC PLUS

K870195 · HPS Unit, Cryophthalmic · Ophthalmic

Feb 1987 31d

SYSTEMS PLUS

K860014 · HQE Instrument, Vitreous... · Ophthalmic

Mar 1986 61d

PARAMETRIC STERILITY RELEASE OF AUTO

K830741 · GAG Stapler, Surgical · General & Plastic Surgery

Aug 1983 156d

United Surgical Corp.

United Surgical Corp. — FDA 510(k) Submissions

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