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FDA 510(k)

CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM

K-Number: K926018 · 1993-03-11

ApplicantBecton Dickinson Microbiology Systems
Decision Date1993-03-11
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM 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 1993-03-11 under 510(k) number K926018. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM?

CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-11. The listed applicant is Becton Dickinson Microbiology Systems. The 510(k) number is K926018.

When did CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM receive FDA 510(k) clearance?

CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM received FDA 510(k) clearance on 1993-03-11, under 510(k) number K926018.

Who is the listed applicant for CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM?

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 CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM?

The FDA product code for CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM is JSS.

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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: JSS)

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.

K123418GRAM-NEGATIVE QUICKFISH BCAdvandx, Inc.K101558GNR TRAFFIC LIGHT PNA FISHAdvandx, Inc.K092236E.COLI/P. AERUGINOSA PNA FISHAdvandx, Inc.K092393EK/P. AERUGINOSA PNA FISHAdvandx, Inc.K082068E. COLI PNA FISHAdvandx, Inc.K081433EK/P. AERUGINOSA PNA FISHAdvandx, 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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