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FDA 510(k)

CANN-HOLD

K-Number: K915057 · 1992-03-19

ApplicantO.R. Concepts, Inc.
Decision Date1992-03-19
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CANN-HOLD is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Concepts, Inc.. It received FDA 510(k) clearance on 1992-03-19 under 510(k) number K915057. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANN-HOLD?

CANN-HOLD is a medical device that received FDA 510(k) clearance on 1992-03-19. The listed applicant is O.R. Concepts, Inc.. The 510(k) number is K915057.

When did CANN-HOLD receive FDA 510(k) clearance?

CANN-HOLD received FDA 510(k) clearance on 1992-03-19, under 510(k) number K915057.

Who is the listed applicant for CANN-HOLD?

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

What is the FDA product code for CANN-HOLD?

The FDA product code for CANN-HOLD is KGX.

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Related Devices (Code: KGX)

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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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