FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HALL OSCILLATOR

K Number: K832187 · Decision Aug 12, 1983
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
22
Applicant Total
19
Review Days
37

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Basic Information

Device Name
HALL OSCILLATOR
K Number
K832187
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Amsco Co.
Date Received
July 6, 1983
Decision Date
August 12, 1983
Product Code
GET
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
GET Motor, Surgical Instrument, Pneumatic Powered

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Other Clearances by Amsco Co.

K Number Device Name
K912471 EAGLE 3000 SDS
K854922 AMSCO POLARIS SL
K833187 HALL OSTEON
K832945 EAGLE 2000 STERILIZER SERIES GAS/AERA
K832188 HALL RECIPROCATOR
K831086 CEILING MOUNTED SUPPORT
K832186 HALL DRILL/REAMER
K831309 DELIVERY 4 TABLE
K823360 SURGICAL LIGHT
K811242 DISPOSABLE STERILIZATION WRAP
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