FDA 510(k)

IPLAN! FLOW

K-Number: K041330 · 2004-09-22

Decision Date2004-09-22

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

IPLAN! FLOW is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2004-09-22 under 510(k) number K041330. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPLAN! FLOW?

IPLAN! FLOW is a medical device that received FDA 510(k) clearance on 2004-09-22. The listed applicant is Brainlab AG. The 510(k) number is K041330.

When did IPLAN! FLOW receive FDA 510(k) clearance?

IPLAN! FLOW received FDA 510(k) clearance on 2004-09-22, under 510(k) number K041330.

Who is the listed applicant for IPLAN! FLOW?

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

What is the FDA product code for IPLAN! FLOW?

The FDA product code for IPLAN! FLOW is HAW.

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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.