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

ISOLIGHT

K Number: K842358 · Decision Jul 31, 1984
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
9
Applicant Total
13
Review Days
39

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Basic Information

Device Name
ISOLIGHT
K Number
K842358
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4630
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Planmeca USA, Inc.
Date Received
June 22, 1984
Decision Date
July 31, 1984
Product Code
EBA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EBA Light, Surgical Headlight

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Other Clearances by Planmeca USA, Inc.

K Number Device Name
K111361 PLANMED NUANCE EXCEL
K081699 PLANMECA SOVEREIGN
K923534 PM2002 PROLINE
K923533 ADMARK
K923462 DELIGHT
K923461 PM2002 PROLINE, PM2002 PROLINE EC
K904953 PLANMED SOPHIE
K904947 PM2002 CC, ARISTOCRAT AND ARISTOCRAT DELUXE
K904948 PM2002 CC AND PM2002 EC
K864474 DENTAL RADIOGRAPHIC 90, MODEL PM 2002 CC PANORAMIC
Search all 13 clearances from Planmeca USA, Inc. →