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)

LOMBARD-DOWELL GLUCOSE AGAR

K-Number: K790626 · 1979-04-23

ApplicantAnaerobe Systems
Decision Date1979-04-23
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LOMBARD-DOWELL GLUCOSE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Anaerobe Systems. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790626. 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 LOMBARD-DOWELL GLUCOSE AGAR?

LOMBARD-DOWELL GLUCOSE AGAR is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Anaerobe Systems. The 510(k) number is K790626.

When did LOMBARD-DOWELL GLUCOSE AGAR receive FDA 510(k) clearance?

LOMBARD-DOWELL GLUCOSE AGAR received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790626.

Who is the listed applicant for LOMBARD-DOWELL GLUCOSE AGAR?

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

What is the FDA product code for LOMBARD-DOWELL GLUCOSE AGAR?

The FDA product code for LOMBARD-DOWELL GLUCOSE AGAR 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 Anaerobe 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.

K844381COLISTIN 10 MCG. DIFFERENTIAL DISKK844382VANCOMYCIN 5MCG DIFFERENTIAL DISKK844383KANAMYCIN 1000 MCG DIFFERENTIAL DISKK844380BILE DIFFERENTIAL DISKK841303CAMPYLOBACTER THIOGLYCOLLATE MEDK841142LEVINE EOSIN METHYLENE BLUE AGAR

View all 52 devices →

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.

↑