VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:— 510(k) K871369

Name: FDA 510(k) clearance K871369
Creator: U.S. Food and Drug Administration
Published: 1987-09-24

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K871369 for VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:, Substantially Equivalent on 1987-09-24. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1987-04-07
Decision date: 1987-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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