Atlas FDA

PARALLEL-A-PREP

FDA 510(k) clearance K801853 · decided 1980-08-13

Clearance details

K-number
K801853
Device name
PARALLEL-A-PREP
Applicant
C.D. Charles, Inc.
Decision
Substantially Equivalent
Date received
1980-08-04
Decision date
1980-08-13
Days to decision
9 days
Clearance type
Traditional
Product code
EGI
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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Recalls involving this device

No recalls on record reference this clearance.