FDA 510(k) Premarket Notification K890935: SYSTEM 3000 FLUIDIZED AIR BED

Submission Details & Decision

Normalized public record details for 510(k) notification K890935.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K890935

Applicant / Sponsor

Dermanetics Corp.

Device Name

SYSTEM 3000 FLUIDIZED AIR BED

Product Code

IOQ

Decision Date

1989-03-15

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Physical Medicine (PM)

Clearance Type

Traditional

Third Party Flag

Date Received

1989-02-24

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