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FDA 510(k)

COUNTER, DISPOSABLE SURGICAL NEEDLE

K-Number: K790039 · 1979-01-17

ApplicantAnago, Inc.
Decision Date1979-01-17
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COUNTER, DISPOSABLE SURGICAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1979-01-17 under 510(k) number K790039. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COUNTER, DISPOSABLE SURGICAL NEEDLE?

COUNTER, DISPOSABLE SURGICAL NEEDLE is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Anago, Inc.. The 510(k) number is K790039.

When did COUNTER, DISPOSABLE SURGICAL NEEDLE receive FDA 510(k) clearance?

COUNTER, DISPOSABLE SURGICAL NEEDLE received FDA 510(k) clearance on 1979-01-17, under 510(k) number K790039.

Who is the listed applicant for COUNTER, DISPOSABLE SURGICAL NEEDLE?

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

What is the FDA product code for COUNTER, DISPOSABLE SURGICAL NEEDLE?

The FDA product code for COUNTER, DISPOSABLE SURGICAL NEEDLE is MMK.

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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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