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FDA 510(k)

PHOS MICROTUBES

K-Number: K812465 · 1981-09-14

ApplicantCarr Microbiologicals
Decision Date1981-09-14
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PHOS MICROTUBES is the device name listed in this FDA 510(k) record. The listed applicant is Carr Microbiologicals. It received FDA 510(k) clearance on 1981-09-14 under 510(k) number K812465. 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 PHOS MICROTUBES?

PHOS MICROTUBES is a medical device that received FDA 510(k) clearance on 1981-09-14. The listed applicant is Carr Microbiologicals. The 510(k) number is K812465.

When did PHOS MICROTUBES receive FDA 510(k) clearance?

PHOS MICROTUBES received FDA 510(k) clearance on 1981-09-14, under 510(k) number K812465.

Who is the listed applicant for PHOS MICROTUBES?

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

What is the FDA product code for PHOS MICROTUBES?

The FDA product code for PHOS MICROTUBES 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Carr Microbiologicals 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.

K812469RAPID DECARBOXYLASE/DIHYDROLASE MICROTUBK812468PYRR MICROTUBEK812470HIPP MICROTUBEK812466ONPX-INDOL MEDIUM MICROTUBESK812467PGUA-INDOL MICROTUBE

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

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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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