E.MEM POWDERED MEDIUM
K-Number: K850232 · 1985-03-07
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Device Summary
Frequently Asked Questions
What is the E.MEM POWDERED MEDIUM?
E.MEM POWDERED MEDIUM is a medical device that received FDA 510(k) clearance on 1985-03-07. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850232.
When did E.MEM POWDERED MEDIUM receive FDA 510(k) clearance?
E.MEM POWDERED MEDIUM received FDA 510(k) clearance on 1985-03-07, under 510(k) number K850232.
Who is the listed applicant for E.MEM POWDERED MEDIUM?
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 E.MEM POWDERED MEDIUM?
The FDA product code for E.MEM POWDERED MEDIUM 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 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: 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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