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FDA 510(k)

UNITED SURGICAL CORP. CRYOPTIC PLUS

K-Number: K870195 · 1987-02-20

ApplicantUnited Surgical Corp.
Decision Date1987-02-20
Product CodeHPS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

UNITED SURGICAL CORP. CRYOPTIC PLUS is the device name listed in this FDA 510(k) record. The listed applicant is United Surgical Corp.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870195. The device is classified under product code HPS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNITED SURGICAL CORP. CRYOPTIC PLUS?

UNITED SURGICAL CORP. CRYOPTIC PLUS is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is United Surgical Corp.. The 510(k) number is K870195.

When did UNITED SURGICAL CORP. CRYOPTIC PLUS receive FDA 510(k) clearance?

UNITED SURGICAL CORP. CRYOPTIC PLUS received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870195.

Who is the listed applicant for UNITED SURGICAL CORP. CRYOPTIC PLUS?

The FDA 510(k) record lists United Surgical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNITED SURGICAL CORP. CRYOPTIC PLUS?

The FDA product code for UNITED SURGICAL CORP. CRYOPTIC PLUS is HPS.

Related Clinical Trials

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Other records listing United Surgical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K902150PIEZO HANDPIECEK870671PHACOTRON DAY PAKK870806NON-STERILE, EXTRA PLUS PAK CAT. #USPK 2100K870194UNITED SURGICAL CORP. DIATHERMIC PLUSK860014SYSTEMS PLUSK830741PARAMETRIC STERILITY RELEASE OF AUTO

View all 7 devices →

Related Devices (Code: HPS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K202038CryoTreQVitreQ BVK940373OPHTHALMIC CRYO UNITDutch Ophthalmic USA, Inc.K923629OPHTHALMIC TRICHIASIS PROBEMira, Inc.K903303SPEMBLY MEDICAL 242 CRYOUNIT/SERIES 242 CRYOPROBESSpembly Medical , Ltd.K874555KEELER ACU 22XT OPHTHALMIC CRYO UNITKeeler Instruments, Inc.K873388KEELER CTU CRYO SYSTEMKeeler Instruments, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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