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FDA 510(k)

BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001

K-Number: K070201 · 2007-08-01

ApplicantC.R. Bard, Inc.
Decision Date2007-08-01
Product CodePHU
DecisionSubstantially Equivalent

Device Summary

BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001 is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2007-08-01 under 510(k) number K070201. The device is classified under product code PHU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001?

BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001 is a medical device that received FDA 510(k) clearance on 2007-08-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K070201.

When did BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001 receive FDA 510(k) clearance?

BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001 received FDA 510(k) clearance on 2007-08-01, under 510(k) number K070201.

Who is the listed applicant for BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001?

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

What is the FDA product code for BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001?

The FDA product code for BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001 is PHU.

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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.

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