ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR
K-Number: K881538 · 1988-04-18
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Device Summary
Frequently Asked Questions
What is the ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR?
ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K881538.
When did ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR receive FDA 510(k) clearance?
ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881538.
Who is the listed applicant for ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR?
The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR?
The FDA product code for ANTIBIOTIC MEDIUM #10 POLYMYXIN SEED AGAR is JSA.
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 Acumedia Manufacturers, 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: JSA)
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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