510(k) K770944
- Device
- INSTATEMP
- Applicant
- H.I. Silverman, D.Sc.
- 510(k) number
- K770944
- Product code
- KDP
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-07-27
- Date received
- 1977-05-25
- Regulation
- 880.6740
- Classification name
- Regulator, Vacuum
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 9680411
- 3007123908
- 3006395447
- 2245304
- 2085602
- 2518417
- 1419185
- 3007360714
- 2221819
- 3011094311
- 2650143
- 2523148
- 3009156722
- 3008812251
- 3005941719
- 3005347827
- 3042172872
- 3005245797
- 3007603826
- 3004530184
- 3009162879
- 3022528821
- 1924066
- 3006897996
- 9610612
- 9611451
- 3008280196
- 1530881
Source Documents#
510(k) summary PDF not indicated by FDA
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