510(k) K770847
- Device
- PORTA-SCALE
- Applicant
- Sr Instruments, Inc.
- 510(k) number
- K770847
- Product code
- FRI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-06-08
- Date received
- 1977-05-09
- Regulation
- 880.2700
- Classification name
- Scale, Stand-On, Patient
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3000122543
- 1423537
- 3010984687
- 3003074886
- 3010895961
- 3007499349
- 3005980667
- 3008386534
- 3004722076
- 3007123908
- 3004018235
- 3014982318
- 3010303097
- 9613910
- 3012302888
- 1054421
- 3004594267
- 3003864328
- 3008262243
- 3007695022
- 3020188747
- 2432177
- 3006624940
- 9680010
- 3008240972
- 1420128
- 3014872855
- 3015236197
- 3008528424
- 3017500903
- 3013689228
- 3011200334
- 3007074192
- 3008973759
- 8030245
- 3017520431
- 8022890
- 8030978
- 1450057
- 3012404027
- 3044174020
- 3013561821
- 3010082909
- 3007649409
- 3008820594
- 3010595915
- 3005374248
- 3021611414
- 3004905643
- 3008717264
- 3007134734
- 3027510187
- 3003587684
- 3013530901
- 1316463
- 3003622639
- 3010381606
- 3001284003
- 1929045
- 3007583504
- 3012724504
- 3005477990
- 3017265430
- 3006570831
- 3007047906
- 3011191255
- 3041928150
- 3004145393
- 3012935929
- 2183494
- 3004128050
- 3003982635
- 3020212802
- 9613926
- 3009456923
- 3013896610
- 3017894657
- 3019300087
- 3007407626
Source Documents#
510(k) summary PDF not indicated by FDA