Atlas FDA

PRESSURE INFUSOR

FDA 510(k) clearance K881977 · decided 1988-07-29

Clearance details

K-number
K881977
Device name
PRESSURE INFUSOR
Applicant
Primrose Medical, Inc.
Decision
Substantially Equivalent
Date received
1988-05-11
Decision date
1988-07-29
Days to decision
79 days
Clearance type
Traditional
Product code
KZD
Device class
1
Regulation number
880.5420
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Woburn, MA, 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
INFUSION DYNAMICS POWER INFUSER (K974074)Infusion Dynamics, Inc.1998-02-17
MSI PRESSURE INFUSOR (K973843)Smith Assoc.1997-10-29
OLYMPUS AUTOMATIC SURGICAL IRRIGATION PUMP (K953290)Olympus America, Inc.1995-10-07
PRESSURIZER (K951988)Promedic, Inc.1995-06-14
PRESSURE INFUSION CUFF (K942933)Circulatory Technology, Inc.1994-08-25
KAWASUMI LABORATORIES K-CUFF (K930012)Kawasumi Laboratories Co., Ltd.1993-12-14
ALLEN INFUSION PUMP MODEL 3000 AND IRRIGATION 2000 (K921168)Allen Medical Systems, Inc.1993-04-21
PRESSURE INFUSER (K913751)Biomedical Dynamics, Inc.1992-01-09
TECNADYNE SURGI-SQUEEZE INFUSION PUMP (K910926)Tecnadyne Scientific, Inc.1991-08-02
INFUSABLE (K911216)Biomedical Dynamics, Inc.1991-07-22
BAXTER SINGLE PATIENT USE PRESSURE INFUSOR (K904484)Tecnadyne Scientific, Inc.1990-10-26
LIFE SHIELD (DISPOSABLE PRESSURE INFUSOR) (K901225)Abbott Laboratories1990-08-23

Recalls involving this device

No recalls on record reference this clearance.