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FDA 510(k)

ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO.

K-Number: K914364 · 1992-09-10

ApplicantNorth American Technical Services Corp.
Decision Date1992-09-10
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO. is the device name listed in this FDA 510(k) record. The listed applicant is North American Technical Services Corp.. It received FDA 510(k) clearance on 1992-09-10 under 510(k) number K914364. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO.?

ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO. is a medical device that received FDA 510(k) clearance on 1992-09-10. The listed applicant is North American Technical Services Corp.. The 510(k) number is K914364.

When did ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO. receive FDA 510(k) clearance?

ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO. received FDA 510(k) clearance on 1992-09-10, under 510(k) number K914364.

Who is the listed applicant for ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO.?

The FDA 510(k) record lists North American Technical Services Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO.?

The FDA product code for ASTOTHERM IFT 250, IFT 260, ASTOTUBE VARIOUS NO. is LGZ.

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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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