FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CipherOx CRI Tablet

K Number: K213255 · Decision Jun 17, 2022
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
7
Applicant Total
3
Review Days
260

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Basic Information

Device Name
CipherOx CRI Tablet
K Number
K213255
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
September 30, 2021
Decision Date
June 17, 2022
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
PPW Adjunctive Cardiovascular Status Indicator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PPW), ordered by most recent decision date.

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Other Clearances by Flashback Technologies, Inc.

K Number Device Name
K173929 CipherOx CRI M1
DEN160020 CipherOx CRI Tablet