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FDA 510(k)

AIRSTRIP OB

K-Number: K090269 · 2009-02-13

ApplicantAirstrip Technologies, LP
Decision Date2009-02-13
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 Airstrip Technologies, LP. It received FDA 510(k) clearance on 2009-02-13 under 510(k) number K090269. 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 2009-02-13. The listed applicant is Airstrip Technologies, LP. The 510(k) number is K090269.

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

AIRSTRIP OB received FDA 510(k) clearance on 2009-02-13, under 510(k) number K090269.

Who is the listed applicant for AIRSTRIP OB?

The FDA 510(k) record lists Airstrip Technologies, 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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Other records listing Airstrip Technologies, LP as applicant

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

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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