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FDA 510(k)

GERM TUBE SOLUTION

K-Number: K884720 · 1989-06-02

ApplicantRemel Co.
Decision Date1989-06-02
Product CodeJXC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GERM TUBE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1989-06-02 under 510(k) number K884720. The device is classified under product code JXC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GERM TUBE SOLUTION?

GERM TUBE SOLUTION is a medical device that received FDA 510(k) clearance on 1989-06-02. The listed applicant is Remel Co.. The 510(k) number is K884720.

When did GERM TUBE SOLUTION receive FDA 510(k) clearance?

GERM TUBE SOLUTION received FDA 510(k) clearance on 1989-06-02, under 510(k) number K884720.

Who is the listed applicant for GERM TUBE SOLUTION?

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 GERM TUBE SOLUTION?

The FDA product code for GERM TUBE SOLUTION is JXC.

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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: JXC)

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.

K960075CHROMAGAR CANDIDAHardy DiagnosticsK913426ALBICANS SUREJrga DiagnosticsK891476C. ALBICANS SCREENCarr-Scarborough Microbiologicals, Inc.K882371SOC SLIDE CULTURE SYSTEMThe Cancer Center AT Wadley InstitutesK832406QUANTUM II YEAST IDENT. SYSTEMAbbott Laboratories

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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