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FDA 510(k)

ANASTOMASIS OCCLUDER

K-Number: K761328 · 1977-02-01

ApplicantMedical Engineering Corp.
Decision Date1977-02-01
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANASTOMASIS OCCLUDER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Corp.. It received FDA 510(k) clearance on 1977-02-01 under 510(k) number K761328. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANASTOMASIS OCCLUDER?

ANASTOMASIS OCCLUDER is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is Medical Engineering Corp.. The 510(k) number is K761328.

When did ANASTOMASIS OCCLUDER receive FDA 510(k) clearance?

ANASTOMASIS OCCLUDER received FDA 510(k) clearance on 1977-02-01, under 510(k) number K761328.

Who is the listed applicant for ANASTOMASIS OCCLUDER?

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

What is the FDA product code for ANASTOMASIS OCCLUDER?

The FDA product code for ANASTOMASIS OCCLUDER is DWS.

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Other records listing Medical Engineering Corp. as applicant

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Related Devices (Code: DWS)

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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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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