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FDA 510(k)

VCARE RETRACTOR/ELEVATOR

K-Number: K071907 · 2007-10-05

ApplicantConmed Corporation
Decision Date2007-10-05
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VCARE RETRACTOR/ELEVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K071907. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VCARE RETRACTOR/ELEVATOR?

VCARE RETRACTOR/ELEVATOR is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Conmed Corporation. The 510(k) number is K071907.

When did VCARE RETRACTOR/ELEVATOR receive FDA 510(k) clearance?

VCARE RETRACTOR/ELEVATOR received FDA 510(k) clearance on 2007-10-05, under 510(k) number K071907.

Who is the listed applicant for VCARE RETRACTOR/ELEVATOR?

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

What is the FDA product code for VCARE RETRACTOR/ELEVATOR?

The FDA product code for VCARE RETRACTOR/ELEVATOR is LKF.

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Related Devices (Code: LKF)

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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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