Atlas FDA

EKH

3 FDA 510(k) clearances · Product code

FDA profile

Official device name
Carver, Dental Amalgam, Operative
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Medical specialty
Dental
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RecordFirmDate
DENTAL INSTRUMENTS - CARVER (K823321)Miltex, Inc.1982-11-24
BEACH AMALGAM CARVER (K821785)Pacific Dental Corp.1982-07-06
PREMIER CARVERS, STYLE #21C & 21D (K780528)Premier Dental Products Co.1978-04-19

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