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FDA 510(k)

WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE

K-Number: K945805 · 1994-12-13

ApplicantWells Johnson Co.
Decision Date1994-12-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Wells Johnson Co.. It received FDA 510(k) clearance on 1994-12-13 under 510(k) number K945805. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE?

WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1994-12-13. The listed applicant is Wells Johnson Co.. The 510(k) number is K945805.

When did WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE receive FDA 510(k) clearance?

WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE received FDA 510(k) clearance on 1994-12-13, under 510(k) number K945805.

Who is the listed applicant for WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE?

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

What is the FDA product code for WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE?

The FDA product code for WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE is GEI.

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Other records listing Wells Johnson Co. as applicant

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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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