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
1335075231
Device Listing 1335075231
Listing Summary
#
Listing key
1335075231
Premarket submission
K911819
Device
ACRA-CUT NEUROLOGICAL SURGICAL DEVICE-POWERED
Applicant
Acra Cut, Inc.
Product code
HBE
Decision date
1991-09-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
30369
1220724
1220724
ACRA CUT, INC.
1
N
2026-01-01
989 MAIN ST. ACTON MA US 01720