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FDA 510(k)

EOSIN METHYLENE BLUE AGAR

K-Number: K820552 · 1982-03-16

Decision Date1982-03-16
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EOSIN METHYLENE BLUE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Supply, Inc.. It received FDA 510(k) clearance on 1982-03-16 under 510(k) number K820552. 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 EOSIN METHYLENE BLUE AGAR?

EOSIN METHYLENE BLUE AGAR is a medical device that received FDA 510(k) clearance on 1982-03-16. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K820552.

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

EOSIN METHYLENE BLUE AGAR received FDA 510(k) clearance on 1982-03-16, under 510(k) number K820552.

Who is the listed applicant for EOSIN METHYLENE BLUE AGAR?

The FDA 510(k) record lists American Laboratory Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for 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.

Other records listing American Laboratory Supply, 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.

View all 36 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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