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FDA 510(k)

GRAB-IT

K-Number: K790367 · 1979-03-02

ApplicantConcept, Inc.
Decision Date1979-03-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRAB-IT is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1979-03-02 under 510(k) number K790367. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAB-IT?

GRAB-IT is a medical device that received FDA 510(k) clearance on 1979-03-02. The listed applicant is Concept, Inc.. The 510(k) number is K790367.

When did GRAB-IT receive FDA 510(k) clearance?

GRAB-IT received FDA 510(k) clearance on 1979-03-02, under 510(k) number K790367.

Who is the listed applicant for GRAB-IT?

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

What is the FDA product code for GRAB-IT?

The FDA product code for GRAB-IT is GEI.

Other records listing Concept, Inc. as applicant

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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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