FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CipherOx CRI M1
K Number: K173929
·
Decision Jul 24, 2018
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
7
Applicant Total
3
Review Days
210
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Basic Information
- Device Name
- CipherOx CRI M1
- K Number
- K173929
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2200
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Flashback Technologies, Inc.
- Date Received
- December 26, 2017
- Decision Date
- July 24, 2018
- Product Code
- PPW
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PPW | Adjunctive Cardiovascular Status Indicator | FDA class 2 | Cardiovascular |
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