HAKOMED ELECDT / PRO ELEDT SERIES— 510(k) K980892

Substantially Equivalent

Alive, Inc.

FDA 510(k) clearance K980892 for HAKOMED ELECDT / PRO ELEDT SERIES, Substantially Equivalent on 1998-05-11. Applicant: Alive, Inc.. Device class: 2.

Clearance details

Applicant: Alive, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1998-03-09
Decision date: 1998-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Honolulu, HI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Alive, Inc.

K980958 — HAKOMED ELECDT/VACUPULLS1998-05-11

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