Atlas FDA

COBE ACCESSORY INTERFACE MODULE (AIM)

FDA 510(k) clearance K861860 · decided 1986-07-18

Clearance details

K-number
K861860
Device name
COBE ACCESSORY INTERFACE MODULE (AIM)
Applicant
Cobe Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1986-05-14
Decision date
1986-07-18
Days to decision
65 days
Clearance type
Traditional
Product code
KRL
Device class
2
Regulation number
870.4205
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Lakewood, CO, US
Third-party review
No
Expedited review
No

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STOCKERT CAPS1 CARDIOPLEGIC CONTROL MODULE (K925661)Sorin Biomedica, Fiat, USA, Inc.1993-05-18
STOCKERT 1/4 BUBBLE SENSOR (K925541)Sorin Biomedica, Fiat, USA, Inc.1993-02-02
CAPIOX(R) BUBBLE TRAP (K911632)Terumo Medical Corp.1991-07-09
CAPS LOW LEVEL DETECTOR & DETECTOR/BUBBLE MONITOR (K864619)Shiley, Inc.1987-02-03
COBE AEPS (K842054)Cobe Laboratories, Inc.1984-08-02

Recalls involving this device

No recalls on record reference this clearance.