FDA 510(k)

AMO PRESTIGE DAY PACK (ALLERGAN, INC.)

K-Number: K962402 · 1996-09-19

Decision Date1996-09-19

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

AMO PRESTIGE DAY PACK (ALLERGAN, INC.) is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1996-09-19 under 510(k) number K962402. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMO PRESTIGE DAY PACK (ALLERGAN, INC.)?

AMO PRESTIGE DAY PACK (ALLERGAN, INC.) is a medical device that received FDA 510(k) clearance on 1996-09-19. The listed applicant is Allergan, Inc.. The 510(k) number is K962402.

When did AMO PRESTIGE DAY PACK (ALLERGAN, INC.) receive FDA 510(k) clearance?

AMO PRESTIGE DAY PACK (ALLERGAN, INC.) received FDA 510(k) clearance on 1996-09-19, under 510(k) number K962402.

Who is the listed applicant for AMO PRESTIGE DAY PACK (ALLERGAN, INC.)?

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 AMO PRESTIGE DAY PACK (ALLERGAN, INC.)?

The FDA product code for AMO PRESTIGE DAY PACK (ALLERGAN, INC.) is HQC.

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Related Devices (Code: HQC)

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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.