SALMONELLA SHIGELLA AGAR
K-Number: K811603 · 1981-06-25
Advertisement
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 1981-06-25. The listed applicant is Micro Media Laboratories. The 510(k) number is K811603.
When did SALMONELLA SHIGELLA AGAR receive FDA 510(k) clearance?
SALMONELLA SHIGELLA AGAR received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811603.
Who is the listed applicant for SALMONELLA SHIGELLA AGAR?
The FDA 510(k) record lists Micro Media Laboratories 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 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 Micro Media Laboratories 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: 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement