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)

BROM CRESOL PURPLE STARCH

K-Number: K851343 · 1985-04-19

ApplicantMicro Media Laboratories
Decision Date1985-04-19
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BROM CRESOL PURPLE STARCH is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1985-04-19 under 510(k) number K851343. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BROM CRESOL PURPLE STARCH?

BROM CRESOL PURPLE STARCH is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is Micro Media Laboratories. The 510(k) number is K851343.

When did BROM CRESOL PURPLE STARCH receive FDA 510(k) clearance?

BROM CRESOL PURPLE STARCH received FDA 510(k) clearance on 1985-04-19, under 510(k) number K851343.

Who is the listed applicant for BROM CRESOL PURPLE STARCH?

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

What is the FDA product code for BROM CRESOL PURPLE STARCH?

The FDA product code for BROM CRESOL PURPLE STARCH is JSH.

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 Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGARK853691TERGITOL 7 AGARK851344OXIDATIVE FORMENTIVE MEDIUMK851345PURPLE BROTHK851348COBA AGARK851347KANAMYCIN-VANCOMYCIN-LAKED BLOOD AGAR

View all 52 devices →

Related Devices (Code: JSH)

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.

K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia 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.

↑