CARDIO2 CYCLE— 510(k) K926233

Substantially Equivalent

Ergometrix, Inc.

FDA 510(k) clearance K926233 for CARDIO2 CYCLE, Substantially Equivalent on 1993-06-04. Applicant: Ergometrix, Inc.. Device class: 1.

Clearance details

Applicant: Ergometrix, Inc.
Product code: Code KRI
Device class: Class 1
Regulation: 21 CFR 870.4200
Advisory panel: Cardiovascular
Date received: 1992-12-11
Decision date: 1993-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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Recent devices under product code KRI

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K990512 — STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS1999-11-23
K934782 — AMMEX TUBING ORGANIZER1993-11-18
K922404 — TUBE GRIP1992-11-23

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