Atlas FDA

PREPARATION, DUPONT

FDA 510(k) clearance K790110 · decided 1979-02-15

Clearance details

K-number
K790110
Device name
PREPARATION, DUPONT
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Decision
Substantially Equivalent
Date received
1979-01-17
Decision date
1979-02-15
Days to decision
29 days
Clearance type
Traditional
Advisory committee
Unknown
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.