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FDA 510(k)

GRAVITY PLUS CONTROLLER/COMPOUNDER

K-Number: K902853 · 1991-05-09

ApplicantFergy Corp.
Decision Date1991-05-09
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRAVITY PLUS CONTROLLER/COMPOUNDER is the device name listed in this FDA 510(k) record. The listed applicant is Fergy Corp.. It received FDA 510(k) clearance on 1991-05-09 under 510(k) number K902853. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAVITY PLUS CONTROLLER/COMPOUNDER?

GRAVITY PLUS CONTROLLER/COMPOUNDER is a medical device that received FDA 510(k) clearance on 1991-05-09. The listed applicant is Fergy Corp.. The 510(k) number is K902853.

When did GRAVITY PLUS CONTROLLER/COMPOUNDER receive FDA 510(k) clearance?

GRAVITY PLUS CONTROLLER/COMPOUNDER received FDA 510(k) clearance on 1991-05-09, under 510(k) number K902853.

Who is the listed applicant for GRAVITY PLUS CONTROLLER/COMPOUNDER?

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

What is the FDA product code for GRAVITY PLUS CONTROLLER/COMPOUNDER?

The FDA product code for GRAVITY PLUS CONTROLLER/COMPOUNDER is LHI.

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Related Devices (Code: LHI)

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.

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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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