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)

EMB AGAR (EOSIN METHYLENE BLUE AGAR)

K-Number: K791520 · 1979-08-22

ApplicantIsle Media and Sterile Products, Inc.
Decision Date1979-08-22
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EMB AGAR (EOSIN METHYLENE BLUE AGAR) is the device name listed in this FDA 510(k) record. The listed applicant is Isle Media and Sterile Products, Inc.. It received FDA 510(k) clearance on 1979-08-22 under 510(k) number K791520. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMB AGAR (EOSIN METHYLENE BLUE AGAR)?

EMB AGAR (EOSIN METHYLENE BLUE AGAR) is a medical device that received FDA 510(k) clearance on 1979-08-22. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K791520.

When did EMB AGAR (EOSIN METHYLENE BLUE AGAR) receive FDA 510(k) clearance?

EMB AGAR (EOSIN METHYLENE BLUE AGAR) received FDA 510(k) clearance on 1979-08-22, under 510(k) number K791520.

Who is the listed applicant for EMB AGAR (EOSIN METHYLENE BLUE AGAR)?

The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMB AGAR (EOSIN METHYLENE BLUE AGAR)?

The FDA product code for EMB AGAR (EOSIN METHYLENE BLUE AGAR) is JSI.

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 Isle Media and Sterile Products, 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.

K831671MODIFIED SOYBEAN CASEIN DIGEST BROTHK821218CAMPY-S AGARK820863MEDIA FOR IN-VITRO DIAGNOSTIC USEK812796ANAEROBIC CNA BLOOD AGARK812795ANAEROBIC BLOOD AGARK812798MOTILITY GI MEDIUM

View all 93 devices →

Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS 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.

↑