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FDA 510(k)

PRECISION MIST COMPRESSOR

K-Number: K923324 · 1993-01-14

Decision Date1993-01-14
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRECISION MIST 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 1993-01-14 under 510(k) number K923324. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION MIST COMPRESSOR?

PRECISION MIST COMPRESSOR is a medical device that received FDA 510(k) clearance on 1993-01-14. The listed applicant is Precision Medical, Inc.. The 510(k) number is K923324.

When did PRECISION MIST COMPRESSOR receive FDA 510(k) clearance?

PRECISION MIST COMPRESSOR received FDA 510(k) clearance on 1993-01-14, under 510(k) number K923324.

Who is the listed applicant for PRECISION MIST 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 PRECISION MIST COMPRESSOR?

The FDA product code for PRECISION MIST COMPRESSOR is CAF.

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: CAF)

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

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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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