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FDA 510(k)

KING KRIB

K-Number: K934298 · 1994-01-26

ApplicantNoritage, Inc.
Decision Date1994-01-26
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KING KRIB is the device name listed in this FDA 510(k) record. The listed applicant is Noritage, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K934298. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KING KRIB?

KING KRIB is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Noritage, Inc.. The 510(k) number is K934298.

When did KING KRIB receive FDA 510(k) clearance?

KING KRIB received FDA 510(k) clearance on 1994-01-26, under 510(k) number K934298.

Who is the listed applicant for KING KRIB?

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

What is the FDA product code for KING KRIB?

The FDA product code for KING KRIB is FNJ.

Related Devices (Code: FNJ)

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.

K892877CRADLE, HOSPITAL BED CLOTHINGWarsaw Orthopedic, Inc.K885241BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MATKing Mfg. Co.K884542SIC 3999 FOLDING ADJUSTABLE HOSPITAL BEDCommercial Products & Engineering Co.K881725ENVIROTENT (BED)Envirotents, Inc.K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64Med Service, Inc.K881964MSI 3003 SERIES BEDMed Service, Inc.

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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