510(k) K780838
- Device
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- Applicant
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- 510(k) number
- K780838
- Product code
- ERROR TEMPORARILY UNAVAILABLE PLEASE SELECT YOUR BACK BUTTON OR CHOOSE A PAGE LISTED BELOW. THANK YOU.
- Decision
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- Decision date
- 1978-07-17
- Date received
- 1978-05-22
- Regulation
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- Classification name
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- Medical specialty
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- Review panel
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- Device class
- 1
- Clearance type
- Error Temporari
- Third party reviewed
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Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3002637618
- 1924066
- 1836161
- 3023162659
- 1219029
- 2183477
Source Documents#
510(k) summary PDF not indicated by FDA