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FDA 510(k)

DIAMOND'S MEDIUM MODIFIED

K-Number: K881995 · 1988-06-02

ApplicantRemel Co.
Decision Date1988-06-02
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIAMOND'S MEDIUM MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1988-06-02 under 510(k) number K881995. The device is classified under product code KZI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMOND'S MEDIUM MODIFIED?

DIAMOND'S MEDIUM MODIFIED is a medical device that received FDA 510(k) clearance on 1988-06-02. The listed applicant is Remel Co.. The 510(k) number is K881995.

When did DIAMOND'S MEDIUM MODIFIED receive FDA 510(k) clearance?

DIAMOND'S MEDIUM MODIFIED received FDA 510(k) clearance on 1988-06-02, under 510(k) number K881995.

Who is the listed applicant for DIAMOND'S MEDIUM MODIFIED?

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

What is the FDA product code for DIAMOND'S MEDIUM MODIFIED?

The FDA product code for DIAMOND'S MEDIUM MODIFIED is KZI.

Related Clinical Trials

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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Other records listing Remel Co. as applicant

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.

K013711BACTI-SWAB DRYK965151A.C.T. IIIK965150A.C.T. IVK965152A.C.T. IIK965149A.C.T. IK960090CALCOFLUOR WHITE STAIN KIT

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Related Devices (Code: KZI)

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.

K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)Oxoid U.S.A., Inc.K880131LOWENSTEIN-JENSEN, GRUFTHardy MediaK880134MIDDLEBROOK 7H11 AGARHardy MediaK880122MIDDLEBROOK 7H9 BROTHHardy MediaK880138WALLENSTEIN MEDIUM SLANTHardy MediaK880109CYSTINE TRYPTIC MEDIUM BASEHardy Media

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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