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FDA 510(k)

ALPHA DUO LAP INSUFFLATOR

K-Number: K090652 · 2009-09-25

ApplicantHippokratec GmbH
Decision Date2009-09-25
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALPHA DUO LAP INSUFFLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Hippokratec GmbH. It received FDA 510(k) clearance on 2009-09-25 under 510(k) number K090652. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALPHA DUO LAP INSUFFLATOR?

ALPHA DUO LAP INSUFFLATOR is a medical device that received FDA 510(k) clearance on 2009-09-25. The listed applicant is Hippokratec GmbH. The 510(k) number is K090652.

When did ALPHA DUO LAP INSUFFLATOR receive FDA 510(k) clearance?

ALPHA DUO LAP INSUFFLATOR received FDA 510(k) clearance on 2009-09-25, under 510(k) number K090652.

Who is the listed applicant for ALPHA DUO LAP INSUFFLATOR?

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

What is the FDA product code for ALPHA DUO LAP INSUFFLATOR?

The FDA product code for ALPHA DUO LAP INSUFFLATOR is HIF.

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Related Devices (Code: HIF)

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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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.

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