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FDA 510(k)

DISPOSABLE NEEDLE COUNTER (20-240)

K-Number: K861316 · 1986-05-02

ApplicantAnago, Inc.
Decision Date1986-05-02
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE NEEDLE COUNTER (20-240) is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K861316. 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 DISPOSABLE NEEDLE COUNTER (20-240)?

DISPOSABLE NEEDLE COUNTER (20-240) is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Anago, Inc.. The 510(k) number is K861316.

When did DISPOSABLE NEEDLE COUNTER (20-240) receive FDA 510(k) clearance?

DISPOSABLE NEEDLE COUNTER (20-240) received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861316.

Who is the listed applicant for DISPOSABLE NEEDLE COUNTER (20-240)?

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 DISPOSABLE NEEDLE COUNTER (20-240)?

The FDA product code for DISPOSABLE NEEDLE COUNTER (20-240) 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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