AUTO TRAUMA KIT— 510(k) K790411

Substantially Equivalent

Marshall Electronics, Inc.

FDA 510(k) clearance K790411 for AUTO TRAUMA KIT, Substantially Equivalent on 1979-06-01. Applicant: Marshall Electronics, Inc.. Device class: 1.

Clearance details

Applicant: Marshall Electronics, Inc.
Product code: Code KME
Device class: Class 1
Regulation: 21 CFR 880.6060
Advisory panel: General Hospital
Date received: 1979-02-26
Decision date: 1979-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code KME

K042145 — READY-HEAT BLANKET2004-09-17
K944953 — OREX MEDICAL BEDDING1994-12-02
K933636 — DISPOSE-A-SHEET1994-01-26
K932539 — DOCTOR DOWN --RESCUE WRAP1993-11-02
K922143 — AMERICAN BURN SHEET1992-08-10

More clearances from Marshall Electronics, Inc.

K813247 — KANESON/COMFORT PLUS MANUAL BREAST PUMP1981-12-03
K780023 — BLACK BAG, ELECTRONIC1978-02-21

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