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

A-DEC 2172 DOCTOR'S UNIT

K Number: K925316 · Decision Dec 9, 1993
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
69
Review Days
414

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Basic Information

Device Name
A-DEC 2172 DOCTOR'S UNIT
K Number
K925316
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
A-Dec, Inc.
Date Received
October 21, 1992
Decision Date
December 9, 1993
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

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Other Clearances by A-Dec, Inc.

K Number Device Name
K213932 A-dec 300, A-dec 500
K133776 A-DEC/W&H ELECTRIC HANDPIECE MOTOR
K102234 A-DEC 200 DENTAL SYSTEM
K100647 A-DEC/W&H SYNEA SONIC SCALER HANDPIECE, MODELS ZA-55, ZA-55 L, ZA-55 LM, ZA-55M, SF1LM
K082716 A-DEC/W&H ALEGRA AIR-DRIVEN HIGHSPEED HANDPIECE, MODEL TE-97, TE-98, A-DEC/W&H ALEGRA HANDPIECE ATTACHMENT, MODEL HE-43
K082827 A-DEC/W&H PROFIN RECIPROCATING CONTRA-ANGLE HANDPIECE ATTACHMENT
K082985 A-DEC 334/335 DELIVERY SYSTEM
K070663 A-DEC/W&H SYNEA AIR-DRIVEN HIGHSPEED HANDPIECE, MODEL TA-98, TA-97, A-DEC/W&H SYNEA HANDPIECE ATTACHMENT
K051657 A-DEC SELF-CONTAINED WATER SYSTEM
K032757 A-DEC SELF-CONTAINED WATER SYSTEM, MODEL 0.7 LITER BOTTLE & 2 LITER BOTTLE
Search all 69 clearances from A-Dec, Inc. →