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FDA 510(k)

COMPRESAID

K-Number: K881516 · 1988-04-29

ApplicantR. Evans Corp.
Decision Date1988-04-29
Product CodeFZF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COMPRESAID is the device name listed in this FDA 510(k) record. The listed applicant is R. Evans Corp.. It received FDA 510(k) clearance on 1988-04-29 under 510(k) number K881516. The device is classified under product code FZF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESAID?

COMPRESAID is a medical device that received FDA 510(k) clearance on 1988-04-29. The listed applicant is R. Evans Corp.. The 510(k) number is K881516.

When did COMPRESAID receive FDA 510(k) clearance?

COMPRESAID received FDA 510(k) clearance on 1988-04-29, under 510(k) number K881516.

Who is the listed applicant for COMPRESAID?

The FDA 510(k) record lists R. Evans Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPRESAID?

The FDA product code for COMPRESAID is FZF.

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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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