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FDA 510(k)

BACTIDROP ACRIDINE ORANGE

K-Number: K920974 · 1992-06-19

ApplicantRemel Co.
Decision Date1992-06-19
Product CodeJFO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BACTIDROP ACRIDINE ORANGE is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1992-06-19 under 510(k) number K920974. The device is classified under product code JFO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTIDROP ACRIDINE ORANGE?

BACTIDROP ACRIDINE ORANGE is a medical device that received FDA 510(k) clearance on 1992-06-19. The listed applicant is Remel Co.. The 510(k) number is K920974.

When did BACTIDROP ACRIDINE ORANGE receive FDA 510(k) clearance?

BACTIDROP ACRIDINE ORANGE received FDA 510(k) clearance on 1992-06-19, under 510(k) number K920974.

Who is the listed applicant for BACTIDROP ACRIDINE ORANGE?

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 ACRIDINE ORANGE?

The FDA product code for BACTIDROP ACRIDINE ORANGE is JFO.

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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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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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