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
1073927722
Device Listing 1073927722
Listing Summary
#
Listing key
1073927722
Premarket submission
K803086
Device
MYOWIRE-ATEMPORARY CARDIAC PACING WIRE
Applicant
Craig & Craig, Inc.
Product code
LDF
Decision date
1981-07-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
6380
2242056
2242056
ALTO DEVELOPMENT CORP.
1
Y
2026-01-01
5206 Asbury Road FARMINGDALE NJ US 07727