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FDA 510(k)

HEPARINIZED WOUND SUCTION TUBING

K-Number: K760812 · 1976-11-03

Decision Date1976-11-03
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEPARINIZED WOUND SUCTION 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 K760812. 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 WOUND SUCTION TUBING?

HEPARINIZED WOUND SUCTION 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 K760812.

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

HEPARINIZED WOUND SUCTION TUBING received FDA 510(k) clearance on 1976-11-03, under 510(k) number K760812.

Who is the listed applicant for HEPARINIZED WOUND SUCTION 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 WOUND SUCTION TUBING?

The FDA product code for HEPARINIZED WOUND SUCTION TUBING is GCX.

Related Clinical Trials

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.

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.

View all 62 devices →

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.

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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