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FDA 510(k)

VMT GENTLE-HALER

K-Number: K842988 · 1984-08-07

ApplicantVortran Medical Technology 1, Inc.
Decision Date1984-08-07
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VMT GENTLE-HALER is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 1984-08-07 under 510(k) number K842988. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VMT GENTLE-HALER?

VMT GENTLE-HALER is a medical device that received FDA 510(k) clearance on 1984-08-07. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K842988.

When did VMT GENTLE-HALER receive FDA 510(k) clearance?

VMT GENTLE-HALER received FDA 510(k) clearance on 1984-08-07, under 510(k) number K842988.

Who is the listed applicant for VMT GENTLE-HALER?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VMT GENTLE-HALER?

The FDA product code for VMT GENTLE-HALER is CCQ.

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Related Devices (Code: CCQ)

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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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