FDA 510(k) Premarket Notification K003939: VENTURE HOME FILL II, MODEL IOH 200

Submission Details & Decision

Normalized public record details for 510(k) notification K003939.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K003939

Applicant / Sponsor

Invacare Corp.

Device Name

VENTURE HOME FILL II, MODEL IOH 200

Product Code

CAW

Decision Date

2001-03-21

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Anesthesiology (AN)

Clearance Type

Traditional

Third Party Flag

Date Received

2000-12-21

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