510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972020Substantially Equivalent

Oscillomate Non-Invasive Blood Pressure Monitor

Cas Medical Systems, Inc., Branford CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972020 is the FDA 510(k) clearance record for OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR, a class II device, cleared for Cas Medical Systems, Inc. on under FDA product code DXW (System, Phonocatheter, Intracavitary). FDA records list 32 510(k) clearances for Cas Medical Systems, Inc., from to . As of , FDA records show no recalls naming K972020.

Clearance record

Decision date
Received
(337 days to decision)
Product code
DXW System, Phonocatheter, Intracavitary
Regulation
21 CFR 870.1270
Device class
Class II
Review panel
Cardiovascular
Applicant
Cas Medical Systems, Inc. 21 Business Park Dr., Branford CT
510(k) summary
Summary
Third party review
No

Clearances, product code DXW

Trailing 12 months

FDA records hold no clearances under product code DXW in the trailing twelve months.

FDA records show no clearances under product code DXW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DXW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260