FDA 510(k) Substantially Equivalent 🇺🇸 United States

LASER ASSISTED SURGICAL LAPAROSCOPY KITS

K Number: K863241 · Decision Sep 12, 1986
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
23
Review Days
21

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
LASER ASSISTED SURGICAL LAPAROSCOPY KITS
K Number
K863241
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Lifestream Int'L, Inc.
Date Received
August 22, 1986
Decision Date
September 12, 1986
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Other Clearances by Lifestream Int'L, Inc.

K Number Device Name
K964571 VISION CARDIOPLEGIA DELIVERY SYSTEM
K962354 DIOMED 15, 30, 60 SURGICAL DIODE LASER
K920178 CARDIOTOMY RESERVOIR W/20 MICRON FILITER
K920618 AUTOTRANSFUSION SUCTION SET
K913181 AUTOLOGOUS BLOOD PROCESSING SYSTEM
K914396 SURGI LIGHT NON-CONTACT FIBERS
K912045 TMP PRESSURE ISOLATORR, TMP PRESSURE MONITOR SYST
K911523 MODIFICATION TO MODEL 90-1460 LASER ADAPTER
K910726 LIGHT-TOUCH AND SURGI LIGHT FIBERS
K904491 TMP LEFT ATRIAL PRESSURE CATH CAT.# 100-00X-000
Search all 23 clearances from Lifestream Int'L, Inc. →