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FDA 510(k)

BACTIDROP NINHYDRIN

K-Number: K920971 · 1992-05-22

ApplicantRemel Co.
Decision Date1992-05-22
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BACTIDROP NINHYDRIN is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1992-05-22 under 510(k) number K920971. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTIDROP NINHYDRIN?

BACTIDROP NINHYDRIN is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Remel Co.. The 510(k) number is K920971.

When did BACTIDROP NINHYDRIN receive FDA 510(k) clearance?

BACTIDROP NINHYDRIN received FDA 510(k) clearance on 1992-05-22, under 510(k) number K920971.

Who is the listed applicant for BACTIDROP NINHYDRIN?

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 BACTIDROP NINHYDRIN?

The FDA product code for BACTIDROP NINHYDRIN is JTO.

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: JTO)

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.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, 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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