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)

MARTIN LEWIS AGAR

K-Number: K850722 · 1985-03-22

ApplicantRapid City Regional Hospital, Inc.
Decision Date1985-03-22
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MARTIN LEWIS AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Rapid City Regional Hospital, Inc.. It received FDA 510(k) clearance on 1985-03-22 under 510(k) number K850722. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN LEWIS AGAR?

MARTIN LEWIS AGAR is a medical device that received FDA 510(k) clearance on 1985-03-22. The listed applicant is Rapid City Regional Hospital, Inc.. The 510(k) number is K850722.

When did MARTIN LEWIS AGAR receive FDA 510(k) clearance?

MARTIN LEWIS AGAR received FDA 510(k) clearance on 1985-03-22, under 510(k) number K850722.

Who is the listed applicant for MARTIN LEWIS AGAR?

The FDA 510(k) record lists Rapid City Regional Hospital, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARTIN LEWIS AGAR?

The FDA product code for MARTIN LEWIS AGAR is JTY.

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 Rapid City Regional Hospital, Inc. 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.

K850724CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIALK850719DNASE TEST MEDIA, CHRISTENSEN'S UREA AGARK850716SELENITE F BROTHK850720EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%K850717AMIES TRANSPORT MEDIAK850721KLIGER'S IRON AGAR, SIM MEDIA, MRVP MEDIUM, BILE E

View all 10 devices →

Related Devices (Code: JTY)

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.

K210511InTray GCBiomed Diagnostics IncorporatedK993033INTRAY GCBiomed Diagnostics, Inc.K954986GC BASE W/ 1% GCHIRemel, L.P.K950196CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIABioclinical Systems, Inc.K933122MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARBioclinical Systems, Inc.K933121MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARBioclinical Systems, 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.

↑