STARKEY MODEL P1 MODULE— 510(k) K873031

Name: FDA 510(k) clearance K873031
Creator: U.S. Food and Drug Administration
Published: 1988-02-08

Substantially Equivalent

Starkey Laboratories, Inc.

FDA 510(k) clearance K873031 for STARKEY MODEL P1 MODULE, Substantially Equivalent on 1988-02-08. Applicant: Starkey Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Starkey Laboratories, Inc.
Product code: Code LRB
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1987-08-04
Decision date: 1988-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

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