Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1819420165
Device Listing 1819420165
Listing Summary
#
Listing key
1819420165
Premarket submission
K982993
Device
PHILIPS OMNIDIAGNOST
Applicant
Philips Medical Systems, Inc.
Product code
OWB
Decision date
1998-09-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
1236
3003768277
3002807880
Maria Heiling
1
N
2026-01-01
3721 Valley Centre Dr. Ste. 500 San Diego CA US 92130