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FDA 510(k)

NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC

K-Number: K863201 · 1986-08-29

ApplicantAllergan, Inc.
Decision Date1986-08-29
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1986-08-29 under 510(k) number K863201. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC?

NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC is a medical device that received FDA 510(k) clearance on 1986-08-29. The listed applicant is Allergan, Inc.. The 510(k) number is K863201.

When did NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC receive FDA 510(k) clearance?

NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC received FDA 510(k) clearance on 1986-08-29, under 510(k) number K863201.

Who is the listed applicant for NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC?

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

What is the FDA product code for NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC?

The FDA product code for NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC is GCY.

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Related Devices (Code: GCY)

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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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