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FDA 510(k)

ANOLIFT - PORTABLE & ANOLIFT - GANTRY

K-Number: K902141 · 1990-09-12

ApplicantAnodyne Corp.
Decision Date1990-09-12
Product CodeFSA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANOLIFT - PORTABLE & ANOLIFT - GANTRY is the device name listed in this FDA 510(k) record. The listed applicant is Anodyne Corp.. It received FDA 510(k) clearance on 1990-09-12 under 510(k) number K902141. The device is classified under product code FSA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANOLIFT - PORTABLE & ANOLIFT - GANTRY?

ANOLIFT - PORTABLE & ANOLIFT - GANTRY is a medical device that received FDA 510(k) clearance on 1990-09-12. The listed applicant is Anodyne Corp.. The 510(k) number is K902141.

When did ANOLIFT - PORTABLE & ANOLIFT - GANTRY receive FDA 510(k) clearance?

ANOLIFT - PORTABLE & ANOLIFT - GANTRY received FDA 510(k) clearance on 1990-09-12, under 510(k) number K902141.

Who is the listed applicant for ANOLIFT - PORTABLE & ANOLIFT - GANTRY?

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

What is the FDA product code for ANOLIFT - PORTABLE & ANOLIFT - GANTRY?

The FDA product code for ANOLIFT - PORTABLE & ANOLIFT - GANTRY is FSA.

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Related Devices (Code: FSA)

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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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