MASTERSCREEN BODY— 510(k) K936108

Substantially Equivalent

Erich Jaeger GmbH & Co. KG

FDA 510(k) clearance K936108 for MASTERSCREEN BODY, Substantially Equivalent on 1995-02-03. Applicant: Erich Jaeger GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Erich Jaeger GmbH & Co. KG
Product code: Code JEH
Device class: Class 2
Regulation: 21 CFR 868.1760
Advisory panel: Anesthesiology
Date received: 1993-12-27
Decision date: 1995-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wuerzburg, Germany, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code JEH

K240706 — PowerCube+ Series (3 models)2024-12-09
K223818 — Model 9160 VitaloQUB2023-05-25
K072061 — MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY2008-04-22
K022636 — BODY BOX 55002003-01-13
K960840 — C.E. VASCULAR MACHINE1997-03-28

More clearances from Erich Jaeger GmbH & Co. KG

K980876 — ASTHMA MONITOR AM21998-08-14
K954140 — MASTERSCREEN IOS1995-12-14
K951901 — MASTERSCREEN PFT BODY1995-07-31

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