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FDA 510(k)

UNITED SURGICAL CORP. DIATHERMIC PLUS

K-Number: K870194 · 1987-02-20

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

Device Summary

UNITED SURGICAL CORP. DIATHERMIC 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 K870194. The device is classified under product code HQR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNITED SURGICAL CORP. DIATHERMIC PLUS?

UNITED SURGICAL CORP. DIATHERMIC 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 K870194.

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

UNITED SURGICAL CORP. DIATHERMIC PLUS received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870194.

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

The FDA product code for UNITED SURGICAL CORP. DIATHERMIC PLUS is HQR.

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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 2100K870195UNITED SURGICAL CORP. CRYOPTIC PLUSK860014SYSTEMS PLUSK830741PARAMETRIC STERILITY RELEASE OF AUTO

View all 7 devices →

Related Devices (Code: HQR)

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.

K050308THERMAL CAUTERY PROBEStarion InstrumentsK990064DI-RHEX OPHTHALMIC DIATHERMY SYSTEMOphthalmic Technologies, Inc.K980522REFRACTEC MCS-100Refractec, Inc.K972749PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S)C.M. Chance , Ltd.K952151STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)StorzK955158SURGITRONEllman Intl., 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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