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FDA 510(k)

COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS

K-Number: K021237 · 2003-04-10

ApplicantCooperSurgical, Inc.
Decision Date2003-04-10
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 2003-04-10 under 510(k) number K021237. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS?

COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K021237.

When did COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 2003-04-10, under 510(k) number K021237.

Who is the listed applicant for COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS?

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

What is the FDA product code for COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS?

The FDA product code for COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS is HET.

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Related Devices (Code: HET)

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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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