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FDA 510(k)

PERCUSSOR

K-Number: K812166 · 1981-08-18

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1981-08-18
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERCUSSOR is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1981-08-18 under 510(k) number K812166. 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 PERCUSSOR?

PERCUSSOR is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K812166.

When did PERCUSSOR receive FDA 510(k) clearance?

PERCUSSOR received FDA 510(k) clearance on 1981-08-18, under 510(k) number K812166.

Who is the listed applicant for PERCUSSOR?

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

What is the FDA product code for PERCUSSOR?

The FDA product code for PERCUSSOR is BYI.

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Other records listing Dhd Medical Products Div. Diemolding Corp. as applicant

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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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