FDA 510(k) FDA class 1 Substantially Equivalent 🇫🇮 Finland

PM2002 PROLINE

K Number: K923534 · Decision Jan 31, 1994
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
13
Review Days
564

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Basic Information

Device Name
PM2002 PROLINE
K Number
K923534
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Planmeca USA, Inc.
Date Received
July 16, 1992
Decision Date
January 31, 1994
Product Code
KLC
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
KLC Chair, Dental, With Operative Unit

Similar 510(k) Clearances

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

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Other Clearances by Planmeca USA, Inc.

K Number Device Name
K111361 PLANMED NUANCE EXCEL
K081699 PLANMECA SOVEREIGN
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
K842359 AUTOMATIC PATIENT CHAIR PM2000 & A
Search all 13 clearances from Planmeca USA, Inc. →