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FDA 510(k)

CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES

K-Number: K030525 · 2003-08-27

ApplicantMid-Atlantic Diagnostics, Inc.
Decision Date2003-08-27
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Mid-Atlantic Diagnostics, Inc.. It received FDA 510(k) clearance on 2003-08-27 under 510(k) number K030525. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES?

CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES is a medical device that received FDA 510(k) clearance on 2003-08-27. The listed applicant is Mid-Atlantic Diagnostics, Inc.. The 510(k) number is K030525.

When did CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES receive FDA 510(k) clearance?

CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES received FDA 510(k) clearance on 2003-08-27, under 510(k) number K030525.

Who is the listed applicant for CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES?

The FDA 510(k) record lists Mid-Atlantic Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES?

The FDA product code for CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES is MQG.

Related Clinical Trials

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Other records listing Mid-Atlantic Diagnostics, Inc. 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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Related Devices (Code: MQG)

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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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