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FDA 510(k)

LAPAROSCOPIC TROCAR STARTER SCALPEL

K-Number: K936154 · 1994-02-04

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1994-02-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC TROCAR STARTER SCALPEL is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1994-02-04 under 510(k) number K936154. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPIC TROCAR STARTER SCALPEL?

LAPAROSCOPIC TROCAR STARTER SCALPEL is a medical device that received FDA 510(k) clearance on 1994-02-04. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K936154.

When did LAPAROSCOPIC TROCAR STARTER SCALPEL receive FDA 510(k) clearance?

LAPAROSCOPIC TROCAR STARTER SCALPEL received FDA 510(k) clearance on 1994-02-04, under 510(k) number K936154.

Who is the listed applicant for LAPAROSCOPIC TROCAR STARTER SCALPEL?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC TROCAR STARTER SCALPEL?

The FDA product code for LAPAROSCOPIC TROCAR STARTER SCALPEL is GCJ.

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Related Devices (Code: GCJ)

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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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