FDA 510(k)

P.O.P. PAIN KIT

K-Number: K001342 · 2000-09-07

Decision Date2000-09-07

Product CodeMEB

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

P.O.P. PAIN KIT is the device name listed in this FDA 510(k) record. The listed applicant is Post Operative Pain Management. It received FDA 510(k) clearance on 2000-09-07 under 510(k) number K001342. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.O.P. PAIN KIT?

P.O.P. PAIN KIT is a medical device that received FDA 510(k) clearance on 2000-09-07. The listed applicant is Post Operative Pain Management. The 510(k) number is K001342.

When did P.O.P. PAIN KIT receive FDA 510(k) clearance?

P.O.P. PAIN KIT received FDA 510(k) clearance on 2000-09-07, under 510(k) number K001342.

Who is the listed applicant for P.O.P. PAIN KIT?

The FDA 510(k) record lists Post Operative Pain Management as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P.O.P. PAIN KIT?

The FDA product code for P.O.P. PAIN KIT is MEB.

Related Devices (Code: MEB)

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.

K250234SMARTeZ™ Elastomeric Infusion Pump (RS series)Epic Medical Pte. , Ltd.K240624InfuLifeFirst Medical Source, LLC K242152SMARTeZ™ Elastomeric Infusion Pump (498111, 498121, 498131, 498141)Epic Medical Pte. , Ltd.K181360ON-Q* Pump with BolusHalyard Health K151650SMARTez elastomeric infusion pumpEpic Medical Pte. , Ltd.K131247MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEMMfs - Medical Flow Systems, Ltd.

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.