FDA 510(k)

OVUM PICK-UP ASPIRATION NEEDLES

K-Number: K983593 · 1999-01-21

Decision Date1999-01-21

Product CodeMQE

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

OVUM PICK-UP ASPIRATION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1999-01-21 under 510(k) number K983593. The device is classified under product code MQE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OVUM PICK-UP ASPIRATION NEEDLES?

OVUM PICK-UP ASPIRATION NEEDLES is a medical device that received FDA 510(k) clearance on 1999-01-21. The listed applicant is Cook Ob/Gyn. The 510(k) number is K983593.

When did OVUM PICK-UP ASPIRATION NEEDLES receive FDA 510(k) clearance?

OVUM PICK-UP ASPIRATION NEEDLES received FDA 510(k) clearance on 1999-01-21, under 510(k) number K983593.

Who is the listed applicant for OVUM PICK-UP ASPIRATION NEEDLES?

The FDA 510(k) record lists Cook Ob/Gyn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OVUM PICK-UP ASPIRATION NEEDLES?

The FDA product code for OVUM PICK-UP ASPIRATION NEEDLES is MQE.

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Related Devices (Code: MQE)

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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.