SIMMONS CITRATE AGAR
K-Number: K851595 · 1985-05-13
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Device Summary
Frequently Asked Questions
What is the SIMMONS CITRATE AGAR?
SIMMONS CITRATE AGAR is a medical device that received FDA 510(k) clearance on 1985-05-13. The listed applicant is Preferred Micro-Media. The 510(k) number is K851595.
When did SIMMONS CITRATE AGAR receive FDA 510(k) clearance?
SIMMONS CITRATE AGAR received FDA 510(k) clearance on 1985-05-13, under 510(k) number K851595.
Who is the listed applicant for SIMMONS CITRATE AGAR?
The FDA 510(k) record lists Preferred Micro-Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIMMONS CITRATE AGAR?
The FDA product code for SIMMONS CITRATE 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 Preferred Micro-Media 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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