CLINITRON ELEXIS— 510(k) K943385

Substantially Equivalent

Ssi Medical Services, Inc.

FDA 510(k) clearance K943385 for CLINITRON ELEXIS, Substantially Equivalent on 1995-02-27. Applicant: Ssi Medical Services, Inc.. Device class: 2.

Clearance details

Applicant: Ssi Medical Services, Inc.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1994-07-13
Decision date: 1995-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Charleston, SC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INX

K972176 — HOME CARE BEAD BED1998-01-16
K964223 — CLINITRON RITE-HITE1997-05-28
K942184 — CLINITRON AT HOME AIR FLUIDED THERAPY1995-02-07
K931168 — X-20 AIR SUPPORT BED1994-02-17
K934689 — LOW AIR LOSS MATTRESS, MODIFICATION1994-02-02

More clearances from Ssi Medical Services, Inc.

K914351 — CLINITRON C-101992-02-14
K890523 — SUPERCAIR1989-02-10
K882161 — ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM1988-07-12
K863047 — FLEXICAIR1986-09-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.