Atlas FDA

PM-3

FDA 510(k) clearance K831750 · decided 1983-07-26

Clearance details

K-number
K831750
Device name
PM-3
Applicant
Delta Medical Industries
Decision
Substantially Equivalent
Date received
1983-06-01
Decision date
1983-07-26
Days to decision
55 days
Clearance type
Traditional
Product code
DXS
Device class
2
Regulation number
870.4310
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, 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
PRESSURE DISPLAY BOX,DLP DISPOSABLE PRESSURE DISPLAY SETS-NON STERILE VERSIONS (K113235)Medtronic, Inc.2011-12-02
VTI DISPOSABLE PRESSURE DISPLAY SET (K944764)Vascular Technology Incorporated1994-12-27
TMP PRESSURE ISOLATORR, TMP PRESSURE MONITOR SYST (K912045)Lifestream Int'L, Inc.1991-10-31
STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR (K900797)Shiley, Inc.1990-05-10
PRESSURE BARRIER KIT CAT. NO. PBK-3 (K873802)American Omni Medical, Inc.1987-11-06
STOCKERT-SHILEY CAPS AND CAPS DUAL PRESSURE MODULE (K862836)Shiley, Inc.1986-09-12
PRESSURE DISPLAY BOX #60000/TUBING SET #61000 (K852232)Dlp, Inc.1985-08-09
PRESSURE MONITOR (K842194)Norton Texas Medical Products1984-08-27
GAMBRO PRESSURE MONITOR PRM 10 (K822822)Gambro, Inc.1982-10-18
PMS-2 PRESSURE MONITOR SEPARATOR (K820912)Delta Medical Industries1982-05-18
CHAMBER, MC-1 DISPOSABLE PRESSURE (K781890)Delta Medical Industries1978-12-04
CORONARY PRESSURE PERFUSION PUMP (K771764)3M Health Care, Sarns1977-09-30

Recalls involving this device

No recalls on record reference this clearance.