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FDA 510(k)

FALCON IVF ONE WELL DISH

K-Number: K991251 · 1999-05-05

Decision Date1999-05-05
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FALCON IVF ONE WELL DISH is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Labware. It received FDA 510(k) clearance on 1999-05-05 under 510(k) number K991251. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FALCON IVF ONE WELL DISH?

FALCON IVF ONE WELL DISH is a medical device that received FDA 510(k) clearance on 1999-05-05. The listed applicant is Becton Dickinson Labware. The 510(k) number is K991251.

When did FALCON IVF ONE WELL DISH receive FDA 510(k) clearance?

FALCON IVF ONE WELL DISH received FDA 510(k) clearance on 1999-05-05, under 510(k) number K991251.

Who is the listed applicant for FALCON IVF ONE WELL DISH?

The FDA 510(k) record lists Becton Dickinson Labware as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FALCON IVF ONE WELL DISH?

The FDA product code for FALCON IVF ONE WELL DISH is MQK.

Related Clinical Trials

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.

Other records listing Becton Dickinson Labware 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.

Related Devices (Code: MQK)

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.

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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