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FDA 510(k)

PERINEOMETER

K-Number: K960311 · 1996-04-18

ApplicantHollister, Inc.
Decision Date1996-04-18
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PERINEOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1996-04-18 under 510(k) number K960311. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERINEOMETER?

PERINEOMETER is a medical device that received FDA 510(k) clearance on 1996-04-18. The listed applicant is Hollister, Inc.. The 510(k) number is K960311.

When did PERINEOMETER receive FDA 510(k) clearance?

PERINEOMETER received FDA 510(k) clearance on 1996-04-18, under 510(k) number K960311.

Who is the listed applicant for PERINEOMETER?

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

What is the FDA product code for PERINEOMETER?

The FDA product code for PERINEOMETER is HIR.

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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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