510(k) K933201

Device
Aesculap Trocar Instrument Set
Applicant
AESCULAP, INC.
510(k) number
K933201
Product code
GCS
Decision
Substantially Equivalent (SESE)
Decision date
1993-09-13
Date received
1993-07-01
Regulation
876.1500
Classification name
Endoscope, Battery-Powered And Accessories
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
VICTORIA MACKINNON
Address
1000 Gateway Blvd. South San Francisco CA US 94080 94080

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code GCS#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K944062LAPRASCOPIC GRASPERInstrument Makar, Inc.1995-02-23
K944067PEANUT WAND, MODIFICATIONIdeal Medical, Inc.1994-12-08
K93276210.0MM SUCTION/IRRIGATION PROBE & TUBING KITInman Medical Corp.1993-08-31
K933371IMC ENDOSCOPIC INSTRUMENT HOLDERInman Medical Corp.1993-08-06
K924134LEISEGANG LAPAROSCOPIC IRRIGATION SYSTEM/ACCESSLeisegang Medical, Inc.1993-07-02
K931340GRASP FORCEPS/SCISSORS/NEEDLE HOLDER/DISSECTORBaxter Healthcare Corp1993-07-01
K925276M.I.S. TROCAR-CANNULAM.I.S. Technology, Inc.1993-05-24
K921006LAPAROSCOPIC RETRACTOR SYSTEMLaparomed Corp.1992-07-28