PHARMA-PLAST CLINIPAK
K-Number: K852443 · 1985-10-16
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Device Summary
Frequently Asked Questions
What is the PHARMA-PLAST CLINIPAK?
PHARMA-PLAST CLINIPAK is a medical device that received FDA 510(k) clearance on 1985-10-16. The listed applicant is Pharma-Plast USA, Inc.. The 510(k) number is K852443.
When did PHARMA-PLAST CLINIPAK receive FDA 510(k) clearance?
PHARMA-PLAST CLINIPAK received FDA 510(k) clearance on 1985-10-16, under 510(k) number K852443.
Who is the listed applicant for PHARMA-PLAST CLINIPAK?
The FDA 510(k) record lists Pharma-Plast USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHARMA-PLAST CLINIPAK?
The FDA product code for PHARMA-PLAST CLINIPAK is FMF.
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 Pharma-Plast USA, 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: FMF)
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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