Atlas FDA

FILLING VOLUME OPTION

FDA 510(k) clearance K882295 · decided 1988-09-13

Clearance details

K-number
K882295
Device name
FILLING VOLUME OPTION
Applicant
Eris Medical Technology
Decision
Substantially Equivalent
Date received
1988-06-02
Decision date
1988-09-13
Days to decision
103 days
Clearance type
Traditional
Product code
LJH
Device class
2
Regulation number
876.5130
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
New Providence, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.