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

AMSCO POLARIS SL

K Number: K854922 · Decision Jan 24, 1986
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
73
Applicant Total
19
Review Days
45

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Basic Information

Device Name
AMSCO POLARIS SL
K Number
K854922
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Amsco Co.
Date Received
December 10, 1985
Decision Date
January 24, 1986
Product Code
FSY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FSY Light, Surgical, Ceiling Mounted

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Other Clearances by Amsco Co.

K Number Device Name
K912471 EAGLE 3000 SDS
K833187 HALL OSTEON
K832945 EAGLE 2000 STERILIZER SERIES GAS/AERA
K832188 HALL RECIPROCATOR
K832187 HALL OSCILLATOR
K831086 CEILING MOUNTED SUPPORT
K832186 HALL DRILL/REAMER
K831309 DELIVERY 4 TABLE
K823360 SURGICAL LIGHT
K811242 DISPOSABLE STERILIZATION WRAP
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