FDA 510(k) Premarket Notification K771407: LUNG VOLUME & PRESSURE MONITOR

Submission Details & Decision

Normalized public record details for 510(k) notification K771407.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K771407

Applicant / Sponsor

Research Development Corp.

Device Name

LUNG VOLUME & PRESSURE MONITOR

Product Code

BZQ

Decision Date

1977-08-04

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Anesthesiology (AN)

Clearance Type

Traditional

Third Party Flag

Date Received

1977-07-29

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