SALMONELLA SHIGELLA AGAR
K-Number: K800982 · 1980-05-23
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Device Summary
Frequently Asked Questions
What is the SALMONELLA SHIGELLA AGAR?
SALMONELLA SHIGELLA AGAR 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 K800982.
When did SALMONELLA SHIGELLA AGAR receive FDA 510(k) clearance?
SALMONELLA SHIGELLA AGAR received FDA 510(k) clearance on 1980-05-23, under 510(k) number K800982.
Who is the listed applicant for SALMONELLA SHIGELLA AGAR?
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 SALMONELLA SHIGELLA AGAR?
The FDA product code for SALMONELLA SHIGELLA AGAR 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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