PMA P800016S014
- Device
- Yennant(tm) & Kelman(tm) Type Ii
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P800016
- Supplement
- S014
- Decision date
- 1989-12-11
Current openFDA PMA Record
- Device
- YENNANT(TM) & KELMAN(TM) TYPE II
- Applicant
- Bausch & Lomb, Inc.
- PMA number
- P800016
- Supplement
- S014
- Product code
- HGL
- Generic name
- Transducer, ultrasonic, obstetric
- Decision date
- 1989-12-11
- Decision code
- APPR
- Date received
- 1989-09-09
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier