CATHETER, MEDIASTINAL&PERICARDIAL— 510(k) K771986

Name: FDA 510(k) clearance K771986
Creator: U.S. Food and Drug Administration
Published: 1977-10-28

Substantially Equivalent

The Minnesota Back Brace Co.

FDA 510(k) clearance K771986 for CATHETER, MEDIASTINAL&PERICARDIAL, Substantially Equivalent on 1977-10-28. Applicant: The Minnesota Back Brace Co.. Device class: 2.

Clearance details

Applicant: The Minnesota Back Brace Co.
Product code: Code FHF
Device class: Class 2
Regulation: 21 CFR 876.4370
Advisory panel: Gastroenterology, Urology
Date received: 1977-10-19
Decision date: 1977-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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