ULTRASONIC TRANSMISSION GEL— 510(k) K884503

Name: FDA 510(k) clearance K884503
Creator: U.S. Food and Drug Administration
Published: 1989-02-13

Substantially Equivalent

Herbert Stanley Co.

FDA 510(k) clearance K884503 for ULTRASONIC TRANSMISSION GEL, Substantially Equivalent on 1989-02-13. Applicant: Herbert Stanley Co.. Device class: 2.

Clearance details

Applicant: Herbert Stanley Co.
Product code: Code JOT
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1988-10-25
Decision date: 1989-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skokie, IL, US

Download summary PDF View on FDA.gov ↗

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K884504 — ELECTRODE GEL1989-03-09

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