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FDA 510(k)

BACTIDROP(TM) LACTOPHENOL ANILINE BLUE

K-Number: K913005 · 1991-09-16

ApplicantRemel Co.
Decision Date1991-09-16
Product CodeJIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BACTIDROP(TM) LACTOPHENOL ANILINE BLUE is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1991-09-16 under 510(k) number K913005. The device is classified under product code JIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTIDROP(TM) LACTOPHENOL ANILINE BLUE?

BACTIDROP(TM) LACTOPHENOL ANILINE BLUE is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Remel Co.. The 510(k) number is K913005.

When did BACTIDROP(TM) LACTOPHENOL ANILINE BLUE receive FDA 510(k) clearance?

BACTIDROP(TM) LACTOPHENOL ANILINE BLUE received FDA 510(k) clearance on 1991-09-16, under 510(k) number K913005.

Who is the listed applicant for BACTIDROP(TM) LACTOPHENOL ANILINE BLUE?

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(TM) LACTOPHENOL ANILINE BLUE?

The FDA product code for BACTIDROP(TM) LACTOPHENOL ANILINE BLUE is JIO.

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.

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.

View all 137 devices →

Related Devices (Code: JIO)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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