BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)

FDA 510(k) Premarket Notification · Submission K020354 · Applicant: Baylis Medical Co., Inc.

Public Record 510(k) Submission Decision Date: 2002-05-03 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K020354.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K020354
Applicant / Sponsor
Device Name
BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)
Product Code
GXD
Decision Date
2002-05-03
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Neurology (NE)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2002-02-04

Related Establishments / Registrations

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