INTERFACE MODULE IDDD— 510(k) K992635

Substantially Equivalent

Stoeckert Instrumente

FDA 510(k) clearance K992635 for INTERFACE MODULE IDDD, Substantially Equivalent on 1999-12-20. Applicant: Stoeckert Instrumente. Device class: 1.

Clearance details

Applicant: Stoeckert Instrumente
Product code: Code KRI
Device class: Class 1
Regulation: 21 CFR 870.4200
Advisory panel: Cardiovascular
Date received: 1999-08-06
Decision date: 1999-12-20
Decision: Substantially Equivalent
Clearance type: Special
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

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K982014 — STOCKERT COMPACT SYSTEM1998-09-04
K972321 — S3 MAST PUMP1998-02-27

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