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FDA 510(k)

SURGICAL DUCT CLAMP (VINE)

K-Number: K882169 · 1988-06-17

ApplicantHenley Intl.
Decision Date1988-06-17
Product CodeGDJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL DUCT CLAMP (VINE) is the device name listed in this FDA 510(k) record. The listed applicant is Henley Intl.. It received FDA 510(k) clearance on 1988-06-17 under 510(k) number K882169. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL DUCT CLAMP (VINE)?

SURGICAL DUCT CLAMP (VINE) is a medical device that received FDA 510(k) clearance on 1988-06-17. The listed applicant is Henley Intl.. The 510(k) number is K882169.

When did SURGICAL DUCT CLAMP (VINE) receive FDA 510(k) clearance?

SURGICAL DUCT CLAMP (VINE) received FDA 510(k) clearance on 1988-06-17, under 510(k) number K882169.

Who is the listed applicant for SURGICAL DUCT CLAMP (VINE)?

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

What is the FDA product code for SURGICAL DUCT CLAMP (VINE)?

The FDA product code for SURGICAL DUCT CLAMP (VINE) is GDJ.

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 Henley Intl. 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 44 devices →

Related Devices (Code: GDJ)

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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