Atlas FDA

ANALYSIS SYSTEM, PREP SAMPLE

FDA 510(k) clearance K781941 · decided 1979-01-03

Clearance details

K-number
K781941
Device name
ANALYSIS SYSTEM, PREP SAMPLE
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Decision
Substantially Equivalent
Date received
1978-11-20
Decision date
1979-01-03
Days to decision
44 days
Clearance type
Traditional
Product code
DOZ
Device class
2
Regulation number
862.3350
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
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.