510(k) K772355
- Device
- BLOOD LINE COMP. NEG. PRESS. PILLOW
- Applicant
- CORDIS CORP.
- 510(k) number
- K772355
- Product code
- FIW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-01-26
- Date received
- 1977-12-27
- Regulation
- 876.5820
- Classification name
- Alarm, Pillow Pressure
- Medical specialty
- Gastroenterology/Urology
- Review panel
- Gastroenterology/Urology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Related Records
Applicant Contact
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents
510(k) summary PDF not indicated by FDA
Legacy Summary
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FDA Review
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