Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TRYPTICASE SOY BROTH BLOOD CULTURE BOTT

K-Number: K812335 · 1981-09-09

ApplicantFisher Scientific Co., LLC
Decision Date1981-09-09
Product CodeJSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRYPTICASE SOY BROTH BLOOD CULTURE BOTT is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1981-09-09 under 510(k) number K812335. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPTICASE SOY BROTH BLOOD CULTURE BOTT?

TRYPTICASE SOY BROTH BLOOD CULTURE BOTT is a medical device that received FDA 510(k) clearance on 1981-09-09. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K812335.

When did TRYPTICASE SOY BROTH BLOOD CULTURE BOTT receive FDA 510(k) clearance?

TRYPTICASE SOY BROTH BLOOD CULTURE BOTT received FDA 510(k) clearance on 1981-09-09, under 510(k) number K812335.

Who is the listed applicant for TRYPTICASE SOY BROTH BLOOD CULTURE BOTT?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRYPTICASE SOY BROTH BLOOD CULTURE BOTT?

The FDA product code for TRYPTICASE SOY BROTH BLOOD CULTURE BOTT is JSC.

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 Fisher Scientific Co., LLC 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.

K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

View all 89 devices →

Related Devices (Code: JSC)

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.

K850143SPORDEX CULTURE MEDIAAmerican Sterilizer Co.K842852BRAIN HEART INFUSION BROTHAnarobe SystemsK842849TRYPTICASE SOY BROTHAnarobe SystemsK841221BRAIN HEART INFUSION BROTHAnaerobe SystemsK841219SHOPPED MEAT CARBOHYDRATEAnaerobe SystemsK833300SABOURAUD BHI AGARAcumedia Manufacturers, 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.

↑