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FDA 510(k)

CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT

K-Number: K000394 · 2000-02-29

ApplicantRocket Medical Plc
Decision Date2000-02-29
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Rocket Medical Plc. It received FDA 510(k) clearance on 2000-02-29 under 510(k) number K000394. 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 CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT?

CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT is a medical device that received FDA 510(k) clearance on 2000-02-29. The listed applicant is Rocket Medical Plc. The 510(k) number is K000394.

When did CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT receive FDA 510(k) clearance?

CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT received FDA 510(k) clearance on 2000-02-29, under 510(k) number K000394.

Who is the listed applicant for CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT?

The FDA 510(k) record lists Rocket Medical Plc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT?

The FDA product code for CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT is MQG.

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Other records listing Rocket Medical Plc as applicant

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Related Devices (Code: MQG)

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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