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FDA 510(k)

MINIMATE COMPRESSOR

K-Number: K051691 · 2005-12-09

Decision Date2005-12-09
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MINIMATE COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 2005-12-09 under 510(k) number K051691. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIMATE COMPRESSOR?

MINIMATE COMPRESSOR is a medical device that received FDA 510(k) clearance on 2005-12-09. The listed applicant is Precision Medical, Inc.. The 510(k) number is K051691.

When did MINIMATE COMPRESSOR receive FDA 510(k) clearance?

MINIMATE COMPRESSOR received FDA 510(k) clearance on 2005-12-09, under 510(k) number K051691.

Who is the listed applicant for MINIMATE COMPRESSOR?

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

What is the FDA product code for MINIMATE COMPRESSOR?

The FDA product code for MINIMATE COMPRESSOR is BTI.

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.

Other records listing Precision Medical, 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.

View all 29 devices →

Related Devices (Code: BTI)

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.

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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