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FDA 510(k)

AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM

K-Number: K051639 · 2005-08-02

ApplicantAs Software, Inc.
Decision Date2005-08-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is As Software, Inc.. It received FDA 510(k) clearance on 2005-08-02 under 510(k) number K051639. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM?

AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM is a medical device that received FDA 510(k) clearance on 2005-08-02. The listed applicant is As Software, Inc.. The 510(k) number is K051639.

When did AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM receive FDA 510(k) clearance?

AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM received FDA 510(k) clearance on 2005-08-02, under 510(k) number K051639.

Who is the listed applicant for AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM?

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

What is the FDA product code for AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM?

The FDA product code for AS-OBGYN INFORMATION SYSTEM; AS-EMR SYSTEM is LLZ.

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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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