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FDA 510(k)

MODEL 7620 LINE CLAMP

K-Number: K792277 · 1980-01-16

Decision Date1980-01-16
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 7620 LINE CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is B-D Drake Willock. It received FDA 510(k) clearance on 1980-01-16 under 510(k) number K792277. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 7620 LINE CLAMP?

MODEL 7620 LINE CLAMP is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is B-D Drake Willock. The 510(k) number is K792277.

When did MODEL 7620 LINE CLAMP receive FDA 510(k) clearance?

MODEL 7620 LINE CLAMP received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792277.

Who is the listed applicant for MODEL 7620 LINE CLAMP?

The FDA 510(k) record lists B-D Drake Willock as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 7620 LINE CLAMP?

The FDA product code for MODEL 7620 LINE CLAMP is KOC.

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.

Related Devices (Code: KOC)

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

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

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