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FDA 510(k)

PHARMAFEED

K-Number: K932649 · 1993-11-16

ApplicantPlasco, Inc.
Decision Date1993-11-16
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHARMAFEED is the device name listed in this FDA 510(k) record. The listed applicant is Plasco, Inc.. It received FDA 510(k) clearance on 1993-11-16 under 510(k) number K932649. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMAFEED?

PHARMAFEED is a medical device that received FDA 510(k) clearance on 1993-11-16. The listed applicant is Plasco, Inc.. The 510(k) number is K932649.

When did PHARMAFEED receive FDA 510(k) clearance?

PHARMAFEED received FDA 510(k) clearance on 1993-11-16, under 510(k) number K932649.

Who is the listed applicant for PHARMAFEED?

The FDA 510(k) record lists Plasco, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHARMAFEED?

The FDA product code for PHARMAFEED is KPE.

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Other records listing Plasco, 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.

K980066CPR FILTERSHIELDK953414CPR MICROMASK WITH OXYGEN INLETK951483CPR MICROMASKK950770CPR MICROSHIELD IIK950769CPR MICROMASK PLUS CATALOG NO 73-402K943386CPR MICROMASK

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Related Devices (Code: KPE)

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.

K252079Disposable Infusion Bag for Parenteral NutritionBeijing L&Z Medical Technology Development Co., Ltd.K251980ClaveQS™ BagIcu Medical, Inc.K251139KabiHelp® Uno; KabiHelp® Advance plusFresenius Kabi AGK252094eZSURE™ Empty Fluid ContainerEpic Medical Pte. , Ltd.K250459DMRX 100ml Empty Container Solution; DMRX 250ml Empty Container Solution; DMRX 500ml Empty Container Solution; DMRX 1000ml Empty Container SolutionTechnoflex Sas.K241442eZSURE™ Empty Fluid Container with ProSeal™ Injection SiteEpic Medical Pte. , Ltd.

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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