PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE
K-Number: K861997 · 1986-06-10
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Device Summary
Frequently Asked Questions
What is the PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE?
PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE is a medical device that received FDA 510(k) clearance on 1986-06-10. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K861997.
When did PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE receive FDA 510(k) clearance?
PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE received FDA 510(k) clearance on 1986-06-10, under 510(k) number K861997.
Who is the listed applicant for PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE?
The FDA 510(k) record lists Hazleton Research Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE?
The FDA product code for PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE is JSK.
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 Hazleton Research Products, 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: JSK)
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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