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FDA 510(k)

MICROMAT W/VARIOUS MODELS

K-Number: K831117 · 1984-05-30

ApplicantPmt, Inc.
Decision Date1984-05-30
Product CodeFNW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROMAT W/VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Pmt, Inc.. It received FDA 510(k) clearance on 1984-05-30 under 510(k) number K831117. The device is classified under product code FNW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMAT W/VARIOUS MODELS?

MICROMAT W/VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Pmt, Inc.. The 510(k) number is K831117.

When did MICROMAT W/VARIOUS MODELS receive FDA 510(k) clearance?

MICROMAT W/VARIOUS MODELS received FDA 510(k) clearance on 1984-05-30, under 510(k) number K831117.

Who is the listed applicant for MICROMAT W/VARIOUS MODELS?

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

What is the FDA product code for MICROMAT W/VARIOUS MODELS?

The FDA product code for MICROMAT W/VARIOUS MODELS is FNW.

Related Clinical Trials

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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Other records listing Pmt, Inc. as applicant

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.

K831118PMT-OPTICA LINEK831119LUO CURRETTES #3211

Related Devices (Code: FNW)

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.

K841183SODIUM CHLORIDE SOLUTION BLOOD CELLReagent Laboratory, Inc.

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.

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