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FDA 510(k)

DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM

K-Number: K813394 · 1982-01-22

ApplicantCox-Uphuff Intl.
Decision Date1982-01-22
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cox-Uphuff Intl.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813394. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM?

DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Cox-Uphuff Intl.. The 510(k) number is K813394.

When did DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM receive FDA 510(k) clearance?

DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813394.

Who is the listed applicant for DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM?

The FDA 510(k) record lists Cox-Uphuff Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM?

The FDA product code for DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM is GCX.

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Other records listing Cox-Uphuff Intl. as applicant

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Related Devices (Code: GCX)

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.

K042454STRYKER CASSETTE PUMPStryker EndoscopyK992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMCircon Corp.K972074SUCTION INSTRUMENTATIONWalter Lorenz Surgical, Inc.K971022CHASE SUCKERChase Medical, Inc.K964127MEDI-VAC FLEXI-CLEAR SUCTION HANDLEAllegiance Healthcare Corp.K964519CURITY THORACENTESIS TRAYKendall Healthcare Products Co. Div.Of Tyco Health

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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