← FDA Medical Device Classifications

Oximeter, Wellness

PGJ · Class II — Moderate Risk (510(k) clearance required) · Cardiovascular · 21 CFR 870.2700

Classification

FDA Product Code
PGJ
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 870.2700
Review panel
AN
Medical specialty
Cardiovascular
Submission type
7
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

Definition

Pulse oximeter intended for wellness use.

Market data

Cleared 510(k) submissions
0
Registered establishments
33

Source

Authoritative
FDA Device Classification database
Machine
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