FDA 510(k) Premarket Notification K873418: BODYLOG STRESS REDUCTION PACKAGE

Submission Details & Decision

Normalized public record details for 510(k) notification K873418.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K873418

Applicant / Sponsor

Bodylog, Inc.

Device Name

BODYLOG STRESS REDUCTION PACKAGE

Product Code

HCC

Decision Date

1987-12-17

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Neurology (NE)

Clearance Type

Traditional

Third Party Flag

Date Received

1987-08-26

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