FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

WatchPAT200U (WP200U)

K Number: K203839 · Decision Mar 21, 2022
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
11
Review Days
446

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Basic Information

Device Name
WatchPAT200U (WP200U)
K Number
K203839
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Itamar Medical , Ltd.
Date Received
December 30, 2020
Decision Date
March 21, 2022
Product Code
MNR
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MNR Ventilatory Effort Recorder

Similar 510(k) Clearances

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

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Other Clearances by Itamar Medical , Ltd.

K Number Device Name
K250460 WatchPAT400 (WP400)
K223675 WatchPAT ONE (WP1)
K211557 EndoPATx
K222331 WatchPAT300 (WP300)
K183559 WatchPAT ONE
K180775 Watch-PAT300
K161579 Watch-PAT200U
K153070 Watch-PAT200U
K133859 WATCH-PAT200U (WP200U)
K102567 WATCH-PAT 200S-3 (WP200S-3)
Search all 11 clearances from Itamar Medical , Ltd. →