FDA 510(k)

VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)

K-Number: K994418 · 2000-01-24

Decision Date2000-01-24

Product CodeHIH

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA) is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2000-01-24 under 510(k) number K994418. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)?

VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA) is a medical device that received FDA 510(k) clearance on 2000-01-24. The listed applicant is ETHICON, Inc.. The 510(k) number is K994418.

When did VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA) receive FDA 510(k) clearance?

VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA) received FDA 510(k) clearance on 2000-01-24, under 510(k) number K994418.

Who is the listed applicant for VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)?

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

What is the FDA product code for VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)?

The FDA product code for VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA) is HIH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.