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FDA 510(k)

AP 34 MULTI-THERAPY INFUSION PUMP

K-Number: K082182 · 2008-08-15

ApplicantQ-Core, Ltd.
Decision Date2008-08-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AP 34 MULTI-THERAPY INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Q-Core, Ltd.. It received FDA 510(k) clearance on 2008-08-15 under 510(k) number K082182. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AP 34 MULTI-THERAPY INFUSION PUMP?

AP 34 MULTI-THERAPY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2008-08-15. The listed applicant is Q-Core, Ltd.. The 510(k) number is K082182.

When did AP 34 MULTI-THERAPY INFUSION PUMP receive FDA 510(k) clearance?

AP 34 MULTI-THERAPY INFUSION PUMP received FDA 510(k) clearance on 2008-08-15, under 510(k) number K082182.

Who is the listed applicant for AP 34 MULTI-THERAPY INFUSION PUMP?

The FDA 510(k) record lists Q-Core, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AP 34 MULTI-THERAPY INFUSION PUMP?

The FDA product code for AP 34 MULTI-THERAPY INFUSION PUMP is FRN.

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.

Related Devices (Code: FRN)

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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