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FDA 510(k)

PERRYMETER(TM)

K-Number: K911190 · 1991-07-26

ApplicantPerrymeter Systems
Decision Date1991-07-26
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PERRYMETER(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Perrymeter Systems. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K911190. 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 PERRYMETER(TM)?

PERRYMETER(TM) is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Perrymeter Systems. The 510(k) number is K911190.

When did PERRYMETER(TM) receive FDA 510(k) clearance?

PERRYMETER(TM) received FDA 510(k) clearance on 1991-07-26, under 510(k) number K911190.

Who is the listed applicant for PERRYMETER(TM)?

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

What is the FDA product code for PERRYMETER(TM)?

The FDA product code for PERRYMETER(TM) is HIR.

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Related Devices (Code: HIR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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