FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KSEA HYDROMAT 263110-20 PRESSURE CHAMBERS AND ACCESSORIES

K Number: K972488 · Decision Jan 22, 1998
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
35
Review Days
204

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
KSEA HYDROMAT 263110-20 PRESSURE CHAMBERS AND ACCESSORIES
K Number
K972488
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Karl Storz Endoscopy
Date Received
July 2, 1997
Decision Date
January 22, 1998
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HET), ordered by most recent decision date.

View all

Other Clearances by Karl Storz Endoscopy

K Number Device Name
K043375 FISCH TITANIUM MIDDLE EAR PROSTHESES
K030848 PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K030009 KSEA POWERSHAVER SYSTEM S2
K023924 AUTOCON II 200 ELECTROSURGICAL GENERATOR
K023187 KSEA SPINOSCOPE
K011700 MODULITH SLK LITHOTRIPTER
K021776 KSEA QUADRO SWITCH
K013107 BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K011841 KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
K010569 KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
Search all 35 clearances from Karl Storz Endoscopy →