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FDA 510(k)

NEEDLE COUNTING

K-Number: K771791 · 1977-10-04

ApplicantChase Mfg. Co.
Decision Date1977-10-04
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLE COUNTING is the device name listed in this FDA 510(k) record. The listed applicant is Chase Mfg. Co.. It received FDA 510(k) clearance on 1977-10-04 under 510(k) number K771791. 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 NEEDLE COUNTING?

NEEDLE COUNTING is a medical device that received FDA 510(k) clearance on 1977-10-04. The listed applicant is Chase Mfg. Co.. The 510(k) number is K771791.

When did NEEDLE COUNTING receive FDA 510(k) clearance?

NEEDLE COUNTING received FDA 510(k) clearance on 1977-10-04, under 510(k) number K771791.

Who is the listed applicant for NEEDLE COUNTING?

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

What is the FDA product code for NEEDLE COUNTING?

The FDA product code for NEEDLE COUNTING is MMK.

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Other records listing Chase Mfg. Co. 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.

K791513ADAMCO DUST COVERK790993INSTANT HOT & COLD PACKSK790644SUBMAXK780033MATTRESSES, CONDUCTIVE & COVERSK771792ENEMA SETK770900CAST BRWM, FRACTURE

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Related Devices (Code: MMK)

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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