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

CAT. 8 DENTAL DEVICES

K Number: K840312 · Decision Apr 5, 1984
Classifications
1
FEI Numbers
210
Registration Numbers
210
Same Product Code
9
Applicant Total
52
Review Days
72

Basic Information

Device Name
CAT. 8 DENTAL DEVICES
K Number
K840312
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
IMM ENTERPRISES LTD.
Date Received
January 24, 1984
Decision Date
April 5, 1984
Product Code
EMG
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
EMG Forceps, Tooth Extractor, Surgical

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K840304 CATEGORY 17-MICROBIOLOGY DEVICES
K840305 CATEGORY 1 CIRCULATORY SYSTEM DEVICE
K840318 CAT. 14-CLINICAL TOXIOLOGY DEVICES
K834171 OP-CON SURG. INSTRUMENT #3
K834192 JAKOBI SURG. INSTRUMENTS #3 21/22/24
K834191 JAKOBI SURGICAL INSTRUMENTS #3 17/18/19
K840310 CATEGORY 6 OPTHALMIC DEVICES
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