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FDA 510(k)

PRE-SERT

K-Number: K822706 · 1982-10-22

ApplicantAllergan, Inc.
Decision Date1982-10-22
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

PRE-SERT is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1982-10-22 under 510(k) number K822706. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-SERT?

PRE-SERT is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Allergan, Inc.. The 510(k) number is K822706.

When did PRE-SERT receive FDA 510(k) clearance?

PRE-SERT received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822706.

Who is the listed applicant for PRE-SERT?

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 PRE-SERT?

The FDA product code for PRE-SERT is HPX.

Other records listing Allergan, Inc. as applicant

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Related Devices (Code: HPX)

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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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