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FDA 510(k)

DB1 EMBRYO FREEZE

K-Number: K011327 · 2002-08-15

ApplicantZander Medical Supplies, Inc.
Decision Date2002-08-15
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DB1 EMBRYO FREEZE is the device name listed in this FDA 510(k) record. The listed applicant is Zander Medical Supplies, Inc.. It received FDA 510(k) clearance on 2002-08-15 under 510(k) number K011327. 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 DB1 EMBRYO FREEZE?

DB1 EMBRYO FREEZE is a medical device that received FDA 510(k) clearance on 2002-08-15. The listed applicant is Zander Medical Supplies, Inc.. The 510(k) number is K011327.

When did DB1 EMBRYO FREEZE receive FDA 510(k) clearance?

DB1 EMBRYO FREEZE received FDA 510(k) clearance on 2002-08-15, under 510(k) number K011327.

Who is the listed applicant for DB1 EMBRYO FREEZE?

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

What is the FDA product code for DB1 EMBRYO FREEZE?

The FDA product code for DB1 EMBRYO FREEZE is MQG.

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Other records listing Zander Medical Supplies, Inc. as applicant

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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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