Atlas FDA

OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR

FDA 510(k) clearance K972020 · decided 1998-05-05

Clearance details

K-number
K972020
Device name
OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR
Applicant
Cas Medical Systems, Inc.
Decision
Substantially Equivalent
Date received
1997-06-02
Decision date
1998-05-05
Days to decision
337 days
Clearance type
Traditional
Product code
DXW
Device class
2
Regulation number
870.1270
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Branford, CT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
NEWMED ABP-LITE (K955887)Newmed Corp.1996-09-05
MILLAR MIKRO-TIP CATHETER PHONOTRANS (K802830)Millar Instruments, Inc.1980-12-10
MODEL 412 ELECTROFLUIDIC MANOMETER (K800222)Med-Tek Corp.1980-02-29
INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR (K800179)Sphygmetrics, Inc.1980-02-11

Recalls involving this device

No recalls on record reference this clearance.