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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceYENNANT(TM) & KELMAN(TM) TYPE II
Generic NameTransducer, ultrasonic, obstetric
Regulation Number884.2960
ApplicantBausch & Lomb, Inc.
1400 N. Goodman St.
Rochester, NY 14609
PMA NumberP800016
Supplement NumberS014
Date Received09/09/1989
Decision Date12/11/1989
Withdrawal Date11/26/2008
Product Code HGL 
Advisory Committee Ophthalmic
Supplement TypeNormal 180 Day Track
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
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