FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MODIFIED CUSHION-FLEX(TM)

K Number: K890108 · Decision Jan 24, 1989
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
50
Applicant Total
29
Review Days
21

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Basic Information

Device Name
MODIFIED CUSHION-FLEX(TM)
K Number
K890108
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5550
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Life Design Systems, Inc.
Date Received
January 3, 1989
Decision Date
January 24, 1989
Product Code
BSJ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BSJ Mask, Gas, Anesthetic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BSJ), ordered by most recent decision date.

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Other Clearances by Life Design Systems, Inc.

K Number Device Name
K913714 MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)
K885313 HUMIDI-FLEX TM
K893030 CHILD SIZE - FILTER FLEX (TM)
K892862 FLEX-CUP PERCUSSOR
K892221 PULMONARY RESUSCITATOR, MODIFICATION
K890011 OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING
K884387 CUSHION FLEX(TM)
K884068 PULMANEX TM (NEO-NATAL SIZE)
K873179 HEATER WIRE BREATHING CIRCUIT
K863857 PULSE-OX
Search all 29 clearances from Life Design Systems, Inc. →