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FDA 510(k)

BBL NINHYDRIN REAGENT DROPPERS

K-Number: K926256 · 1993-01-26

ApplicantBecton Dickinson Microbiology Systems
Decision Date1993-01-26
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BBL NINHYDRIN REAGENT DROPPERS is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Microbiology Systems. It received FDA 510(k) clearance on 1993-01-26 under 510(k) number K926256. 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 BBL NINHYDRIN REAGENT DROPPERS?

BBL NINHYDRIN REAGENT DROPPERS is a medical device that received FDA 510(k) clearance on 1993-01-26. The listed applicant is Becton Dickinson Microbiology Systems. The 510(k) number is K926256.

When did BBL NINHYDRIN REAGENT DROPPERS receive FDA 510(k) clearance?

BBL NINHYDRIN REAGENT DROPPERS received FDA 510(k) clearance on 1993-01-26, under 510(k) number K926256.

Who is the listed applicant for BBL NINHYDRIN REAGENT DROPPERS?

The FDA 510(k) record lists Becton Dickinson Microbiology Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BBL NINHYDRIN REAGENT DROPPERS?

The FDA product code for BBL NINHYDRIN REAGENT DROPPERS is JTO.

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Other records listing Becton Dickinson Microbiology Systems 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.

K993577CEFOTAXIME/CLAVULANIC, 30/10UG, BBL SENSI-DISC AND CEFTAZIDIME/CLAVULANIC ACID, 30/10UG, BBL SENSI-DISCK984631BDPROBETEC ET CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE AMPLIFIED DNA ASSAYK981517CEFDINIR, 5 UG, SENSI-DISCK980683TROVAFLOXACIN 10G, SENSI-DISCK974578GREPAFLOXACIN, 5 MG, SENSI-DISCK970333BACTEC MYCO/F LYTIC CULTURE VIALS

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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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