Atlas FDA

DENTAL INSTRUMENTS - CARVER

FDA 510(k) clearance K823321 · decided 1982-11-24

Clearance details

K-number
K823321
Device name
DENTAL INSTRUMENTS - CARVER
Applicant
Miltex, Inc.
Decision
Substantially Equivalent
Date received
1982-11-08
Decision date
1982-11-24
Days to decision
16 days
Clearance type
Traditional
Product code
EKH
Device class
1
Regulation number
872.4565
Medical specialty
Dental
Advisory committee
Dental
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
BEACH AMALGAM CARVER (K821785)Pacific Dental Corp.1982-07-06
PREMIER CARVERS, STYLE #21C & 21D (K780528)Premier Dental Products Co.1978-04-19

Recalls involving this device

No recalls on record reference this clearance.