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FDA 510(k)

EOSIN METHYLENE BLUE AGAR, LEVINE

K-Number: K800984 · 1980-05-23

Decision Date1980-05-23
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EOSIN METHYLENE BLUE AGAR, LEVINE is the device name listed in this FDA 510(k) record. The listed applicant is Quality Assurance Laboratory, Inc.. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K800984. 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 EOSIN METHYLENE BLUE AGAR, LEVINE?

EOSIN METHYLENE BLUE AGAR, LEVINE is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Quality Assurance Laboratory, Inc.. The 510(k) number is K800984.

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

EOSIN METHYLENE BLUE AGAR, LEVINE received FDA 510(k) clearance on 1980-05-23, under 510(k) number K800984.

Who is the listed applicant for EOSIN METHYLENE BLUE AGAR, LEVINE?

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

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

The FDA product code for EOSIN METHYLENE BLUE AGAR, LEVINE 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.

Other records listing Quality Assurance Laboratory, 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 11 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.

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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