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FDA 510(k)

CAP, TAMPER PROOF PLASTIC

K-Number: K782113 · 1979-06-01

ApplicantAcacia, Inc.
Decision Date1979-06-01
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CAP, TAMPER PROOF PLASTIC is the device name listed in this FDA 510(k) record. The listed applicant is Acacia, Inc.. It received FDA 510(k) clearance on 1979-06-01 under 510(k) number K782113. 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 CAP, TAMPER PROOF PLASTIC?

CAP, TAMPER PROOF PLASTIC is a medical device that received FDA 510(k) clearance on 1979-06-01. The listed applicant is Acacia, Inc.. The 510(k) number is K782113.

When did CAP, TAMPER PROOF PLASTIC receive FDA 510(k) clearance?

CAP, TAMPER PROOF PLASTIC received FDA 510(k) clearance on 1979-06-01, under 510(k) number K782113.

Who is the listed applicant for CAP, TAMPER PROOF PLASTIC?

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

What is the FDA product code for CAP, TAMPER PROOF PLASTIC?

The FDA product code for CAP, TAMPER PROOF PLASTIC is KPE.

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Other records listing Acacia, 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.

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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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