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FDA 510(k)

PHARMA-PLAST CLINIPAK

K-Number: K852443 · 1985-10-16

Decision Date1985-10-16
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHARMA-PLAST CLINIPAK is the device name listed in this FDA 510(k) record. The listed applicant is Pharma-Plast USA, Inc.. It received FDA 510(k) clearance on 1985-10-16 under 510(k) number K852443. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 9 devices →

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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