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FDA 510(k)

HEPARINIZED PENROSE TUBING

K-Number: K760814 · 1976-11-03

ApplicantSherwood Medical Industries
Decision Date1976-11-03
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEPARINIZED PENROSE TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-11-03 under 510(k) number K760814. 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 HEPARINIZED PENROSE TUBING?

HEPARINIZED PENROSE TUBING is a medical device that received FDA 510(k) clearance on 1976-11-03. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760814.

When did HEPARINIZED PENROSE TUBING receive FDA 510(k) clearance?

HEPARINIZED PENROSE TUBING received FDA 510(k) clearance on 1976-11-03, under 510(k) number K760814.

Who is the listed applicant for HEPARINIZED PENROSE TUBING?

The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEPARINIZED PENROSE TUBING?

The FDA product code for HEPARINIZED PENROSE TUBING is GCX.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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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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