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FDA 510(k)

HAEMOPHILUS TEST MEDIUM (AGAR)

K-Number: K892928 · 1989-06-13

ApplicantRemel Co.
Decision Date1989-06-13
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HAEMOPHILUS TEST MEDIUM (AGAR) is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1989-06-13 under 510(k) number K892928. The device is classified under product code JSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAEMOPHILUS TEST MEDIUM (AGAR)?

HAEMOPHILUS TEST MEDIUM (AGAR) is a medical device that received FDA 510(k) clearance on 1989-06-13. The listed applicant is Remel Co.. The 510(k) number is K892928.

When did HAEMOPHILUS TEST MEDIUM (AGAR) receive FDA 510(k) clearance?

HAEMOPHILUS TEST MEDIUM (AGAR) received FDA 510(k) clearance on 1989-06-13, under 510(k) number K892928.

Who is the listed applicant for HAEMOPHILUS TEST MEDIUM (AGAR)?

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 HAEMOPHILUS TEST MEDIUM (AGAR)?

The FDA product code for HAEMOPHILUS TEST MEDIUM (AGAR) is JSO.

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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: JSO)

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.

K190553HardyCHROM CREHardy DiagnosticsK181092CHROMID CARBA agar (CARB)Biomerieux S.A.K171061MRSASelect IIBio-RadK162620Remel Spectra ESBLRemel, Inc.K160512HardyCHROM ESBLHardy DiagnosticsK162076chromID MRSAbioMerieux, Inc.

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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