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FDA 510(k)

MANUAL PERCUSSOR CUPS

K-Number: K883899 · 1988-12-13

ApplicantMedical Components, Inc.
Decision Date1988-12-13
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MANUAL PERCUSSOR CUPS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1988-12-13 under 510(k) number K883899. 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 MANUAL PERCUSSOR CUPS?

MANUAL PERCUSSOR CUPS is a medical device that received FDA 510(k) clearance on 1988-12-13. The listed applicant is Medical Components, Inc.. The 510(k) number is K883899.

When did MANUAL PERCUSSOR CUPS receive FDA 510(k) clearance?

MANUAL PERCUSSOR CUPS received FDA 510(k) clearance on 1988-12-13, under 510(k) number K883899.

Who is the listed applicant for MANUAL PERCUSSOR CUPS?

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

What is the FDA product code for MANUAL PERCUSSOR CUPS?

The FDA product code for MANUAL PERCUSSOR CUPS is BYI.

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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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