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YENNANT(TM) & KELMAN(TM) TYPE II

FDA premarket approval P800016/S014 · decided 1989-12-11

Approval details

PMA number
P800016
Supplement
S014
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
YENNANT(TM) & KELMAN(TM) TYPE II
Generic name
Transducer, ultrasonic, obstetric
Applicant
Bausch & Lomb, Inc.
Date received
1989-09-09
Decision date
1989-12-11
Days to decision
93 days
Decision code
APPR
Product code
HGL
Advisory committee
Ophthalmic
Expedited review
No
Location
Rochester, NY

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