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

SHARPLAN SMOKE EVACUATION UNIT, MODEL 100

K Number: K894765 · Decision Sep 28, 1989
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
20
Review Days
64

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
SHARPLAN SMOKE EVACUATION UNIT, MODEL 100
K Number
K894765
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Laser Industries , Ltd.
Date Received
July 26, 1989
Decision Date
September 28, 1989
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Laser Industries , Ltd.

K Number Device Name
K933362 SHARPLAN CO2 SURGICAL LASER
K850628 SHARPLAN 1040 CO/2 SURGICAL LASER
K850633 SHARPLAN MODEL 1060 CO/2 SURGICAL LASER
K842997 LASER RECTOSCOPE SET 784
K832550 SHARPLAN #734 LASER SURGICAL UNIT
K832551 SHARPLAN #745 LASER SURG. UNIT
K832316 OPHTHALMIC ARGON LASER #700A
K837573 SHARPLAN LASER POSITIONING SYSTEM
K837342 SHARPLAN 721 CO2 SURGICAL LASER
K837081 MICROSCAN 771 MANIPULATOR
Search all 20 clearances from Laser Industries , Ltd. →