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FDA 510(k)

HAND PERCUSSOR CUP #65210

K-Number: K802646 · 1980-11-12

ApplicantB & F Medical Products, Inc.
Decision Date1980-11-12
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HAND PERCUSSOR CUP #65210 is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802646. 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 HAND PERCUSSOR CUP #65210?

HAND PERCUSSOR CUP #65210 is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K802646.

When did HAND PERCUSSOR CUP #65210 receive FDA 510(k) clearance?

HAND PERCUSSOR CUP #65210 received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802646.

Who is the listed applicant for HAND PERCUSSOR CUP #65210?

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

What is the FDA product code for HAND PERCUSSOR CUP #65210?

The FDA product code for HAND PERCUSSOR CUP #65210 is BYI.

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Other records listing B & F Medical Products, Inc. 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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