PHASIS ELECTROMYOGRAPH— 510(k) K922488

Substantially Equivalent

Biosound, Inc.

FDA 510(k) clearance K922488 for PHASIS ELECTROMYOGRAPH, Substantially Equivalent on 1993-03-02. Applicant: Biosound, Inc.. Device class: 2.

Clearance details

Applicant: Biosound, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1992-05-27
Decision date: 1993-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Biosound, Inc.

K971700 — BIOPSY ACCESSORY FOR ULTRASOUND TRANSDUCER1997-07-09
K963936 — ACCESSPOINT, MED E-MAIL, DICOM READER1997-03-31
K963262 — ARTOSCAN M1997-03-28
K963662 — GALILEO EVOKED POTENTIALRE1997-02-26
K953716 — INTRACAVITY TRANSDUCERS1996-04-17

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