PENICILLIN/STREPTOMYCIN SOLUTION
K-Number: K854567 · 1985-12-06
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Device Summary
Frequently Asked Questions
What is the PENICILLIN/STREPTOMYCIN SOLUTION?
PENICILLIN/STREPTOMYCIN SOLUTION is a medical device that received FDA 510(k) clearance on 1985-12-06. The listed applicant is Mediatech, Inc.. The 510(k) number is K854567.
When did PENICILLIN/STREPTOMYCIN SOLUTION receive FDA 510(k) clearance?
PENICILLIN/STREPTOMYCIN SOLUTION received FDA 510(k) clearance on 1985-12-06, under 510(k) number K854567.
Who is the listed applicant for PENICILLIN/STREPTOMYCIN SOLUTION?
The FDA 510(k) record lists Mediatech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PENICILLIN/STREPTOMYCIN SOLUTION?
The FDA product code for PENICILLIN/STREPTOMYCIN SOLUTION is KIT.
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 Mediatech, 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: KIT)
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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