510(k) K760944
- Device
- ANGIOGRAPHIC GUIDEWIRE
- Applicant
- Medrad, Inc.
- 510(k) number
- K760944
- Product code
- DQX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-12-10
- Date received
- 1976-11-01
- Regulation
- 870.1330
- Classification name
- Wire, Guide, Catheter
- Medical specialty
- Cardiovascular
- Review panel
- Cardiovascular
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Related Records
Applicant Contact
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers
- 3000247873
- 1000563940
- 3015173212
- 3012050423
- 1028232
- 1423537
- 2024311
- 3008061490
- 3007113487
- 3007146453
- 3006425876
- 3003898360
- 2029275
- 2024024
- 3007284006
- 1056553
- 2528981
- 3012223769
- 3013288201
- 3014656749
- 3013656790
- 3010532612
- 3008363989
- 2939520
- 1649869
- 2134244
- 2017865
- 3026317086
- 3002807314
- 3010882065
- 3002244583
- 3030574705
- 3027260597
- 1118880
- 1625425
- 3015531723
- 9611446
- 3007628272
- 1000121056
- 3009600098
- 3012154226
- 3008988055
- 3008627763
- 3011050570
- 3007830707
- 2025587
- 3006010712
- 3013162291
- 9616088
- 3002808486
- 3007064586
- 2011171
- 3004784537
- 9610139
- 3014246639
- 3012497308
- 1222301
- 1048735
- 3036802499
- 1319639
- 3013943846
- 3003775027
- 2126666
- 1018233
- 1054241
- 3005737652
- 3008853977
- 1928237
- 3012931345
- 2182208
- 3003915875
- 2135147
- 1225687
- 1018470
- 3011706110
- 9614758
- 3017636737
- 1064858
- 3007138831
Source Documents
510(k) summary PDF not indicated by FDA
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