FDA 510(k)

PHARMA-PLAST INSULIN INFUSION SET

K-Number: K884978 · 1989-06-21

Decision Date1989-06-21

Product CodeLZG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PHARMA-PLAST INSULIN INFUSION SET 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 1989-06-21 under 510(k) number K884978. The device is classified under product code LZG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMA-PLAST INSULIN INFUSION SET?

PHARMA-PLAST INSULIN INFUSION SET is a medical device that received FDA 510(k) clearance on 1989-06-21. The listed applicant is Pharma-Plast USA, Inc.. The 510(k) number is K884978.

When did PHARMA-PLAST INSULIN INFUSION SET receive FDA 510(k) clearance?

PHARMA-PLAST INSULIN INFUSION SET received FDA 510(k) clearance on 1989-06-21, under 510(k) number K884978.

Who is the listed applicant for PHARMA-PLAST INSULIN INFUSION SET?

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 INSULIN INFUSION SET?

The FDA product code for PHARMA-PLAST INSULIN INFUSION SET is LZG.

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Related Devices (Code: LZG)

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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.