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FDA 510(k)

MICRODILUTION ANAEROBE ID. PANEL

K-Number: K781369 · 1978-10-03

ApplicantCnr Labs
Decision Date1978-10-03
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICRODILUTION ANAEROBE ID. PANEL is the device name listed in this FDA 510(k) record. The listed applicant is Cnr Labs. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K781369. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRODILUTION ANAEROBE ID. PANEL?

MICRODILUTION ANAEROBE ID. PANEL is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Cnr Labs. The 510(k) number is K781369.

When did MICRODILUTION ANAEROBE ID. PANEL receive FDA 510(k) clearance?

MICRODILUTION ANAEROBE ID. PANEL received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781369.

Who is the listed applicant for MICRODILUTION ANAEROBE ID. PANEL?

The FDA 510(k) record lists Cnr Labs as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRODILUTION ANAEROBE ID. PANEL?

The FDA product code for MICRODILUTION ANAEROBE ID. PANEL is JSF.

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 Cnr Labs 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.

K792647AUTOSCAN 3K781368MICRODILUTION GRAM-NEGATIVE ID. PANELK781367MICRODILUTION STREP ID. PANEL

Related Devices (Code: JSF)

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.

K880946NUTRIENT GELATIN - PRODUCT NUMBER T2860Lakewood Biochemical Co., Inc.K880126LAURYL TRYPTOSE BROTHHardy MediaK880119MOELLERS DECARBOXYLASE, ONITHINEHardy MediaK880120MOELLERS DECARBOXYLASE, LYSINEHardy MediaK880139ONPG TEST REAGENTHardy MediaK880113CYSTINE TRYPTIC MEDIUM W/LACTOSEHardy Media

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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