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FDA 510(k)

PENICILLIN/STREPTOMYCIN SOLUTION

K-Number: K854567 · 1985-12-06

Decision Date1985-12-06
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PENICILLIN/STREPTOMYCIN SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Mediatech, Inc.. It received FDA 510(k) clearance on 1985-12-06 under 510(k) number K854567. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 24 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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