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FDA 510(k)

THE MCSHIRLEY PERCUSSOR

K-Number: K801982 · 1980-09-16

ApplicantMcshirley Products, Inc.
Decision Date1980-09-16
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE MCSHIRLEY PERCUSSOR is the device name listed in this FDA 510(k) record. The listed applicant is Mcshirley Products, Inc.. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801982. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MCSHIRLEY PERCUSSOR?

THE MCSHIRLEY PERCUSSOR is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Mcshirley Products, Inc.. The 510(k) number is K801982.

When did THE MCSHIRLEY PERCUSSOR receive FDA 510(k) clearance?

THE MCSHIRLEY PERCUSSOR received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801982.

Who is the listed applicant for THE MCSHIRLEY PERCUSSOR?

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

What is the FDA product code for THE MCSHIRLEY PERCUSSOR?

The FDA product code for THE MCSHIRLEY PERCUSSOR is BYI.

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Other records listing Mcshirley Products, Inc. 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: BYI)

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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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