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FDA 510(k)

INSTRUMENTS FOR MICRO ANASTOMOSIS

K-Number: K843100 · 1984-09-27

Decision Date1984-09-27
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENTS FOR MICRO ANASTOMOSIS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1984-09-27 under 510(k) number K843100. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENTS FOR MICRO ANASTOMOSIS?

INSTRUMENTS FOR MICRO ANASTOMOSIS is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K843100.

When did INSTRUMENTS FOR MICRO ANASTOMOSIS receive FDA 510(k) clearance?

INSTRUMENTS FOR MICRO ANASTOMOSIS received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843100.

Who is the listed applicant for INSTRUMENTS FOR MICRO ANASTOMOSIS?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENTS FOR MICRO ANASTOMOSIS?

The FDA product code for INSTRUMENTS FOR MICRO ANASTOMOSIS is GAD.

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 Downs Surgical , Ltd. 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.

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Related Devices (Code: GAD)

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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