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FDA 510(k)

AIRSTRIP OB

K-Number: K042082 · 2005-01-21

ApplicantMp4 Solutions, LP
Decision Date2005-01-21
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AIRSTRIP OB is the device name listed in this FDA 510(k) record. The listed applicant is Mp4 Solutions, LP. It received FDA 510(k) clearance on 2005-01-21 under 510(k) number K042082. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRSTRIP OB?

AIRSTRIP OB is a medical device that received FDA 510(k) clearance on 2005-01-21. The listed applicant is Mp4 Solutions, LP. The 510(k) number is K042082.

When did AIRSTRIP OB receive FDA 510(k) clearance?

AIRSTRIP OB received FDA 510(k) clearance on 2005-01-21, under 510(k) number K042082.

Who is the listed applicant for AIRSTRIP OB?

The FDA 510(k) record lists Mp4 Solutions, LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRSTRIP OB?

The FDA product code for AIRSTRIP OB is HGM.

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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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