CUSHION FLEX(TM)— 510(k) K884387

Substantially Equivalent

Life Design Systems, Inc.

FDA 510(k) clearance K884387 for CUSHION FLEX(TM), Substantially Equivalent on 1988-11-17. Applicant: Life Design Systems, Inc.. Device class: 1.

Clearance details

Applicant: Life Design Systems, Inc.
Product code: Code BSJ
Device class: Class 1
Regulation: 21 CFR 868.5550
Advisory panel: Anesthesiology
Date received: 1988-10-18
Decision date: 1988-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin, WI, US

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More clearances from Life Design Systems, Inc.

K913714 — MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)1992-12-01
K885313 — HUMIDI-FLEX TM1989-10-11
K893030 — CHILD SIZE - FILTER FLEX (TM)1989-09-18
K892862 — FLEX-CUP PERCUSSOR1989-05-25
K892221 — PULMONARY RESUSCITATOR, MODIFICATION1989-05-18

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