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

MICROFIL CONTOURING INSTRUMENTS

K Number: K830776 · Decision Apr 28, 1983
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
4
Applicant Total
21
Review Days
48

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Basic Information

Device Name
MICROFIL CONTOURING INSTRUMENTS
K Number
K830776
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Almore Intl., Inc.
Date Received
March 11, 1983
Decision Date
April 28, 1983
Product Code
EIY
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
EIY Instrument, Filling, Plastic, Dental

Similar 510(k) Clearances

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Other Clearances by Almore Intl., Inc.

K Number Device Name
K862851 ALMORE FACE MASK
K854692 MONARCH II BLEACHING INSTRUMENT
K854696 OP II VISIBLE LIGHT CURING SYSTEM
K854690 DIAMONDS BURS-COMPOSIT FINISHING
K854691 DIAMOND BURS-HANDPIECE
K854700 EZ-ON TUBING CONDITIONER (LUBRICANT)
K854702 PLASTIC MOUNTING RINGS
K854701 RETRACT-A-CORD
K854697 TUBING HANDPIECE REPLACEMENT
K854699 TUBING SYRING
Search all 21 clearances from Almore Intl., Inc. →