LIQUID OXYGEN STORAGE SUBSYSTEM

FDA 510(k) Premarket Notification · Submission K941819 · Applicant: Hogan & Hartson

Public Record 510(k) Submission Decision Date: 1994-05-23 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K941819.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K941819

Applicant / Sponsor

Hogan & Hartson

Device Name

LIQUID OXYGEN STORAGE SUBSYSTEM

Product Code

BYJ

Decision Date

1994-05-23

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Anesthesiology (AN)

Clearance Type

Traditional

Third Party Flag

Date Received

1994-04-13

Related Establishments / Registrations

Essex Industries, Inc Registration: 1937980 View Registration
CAIRE INC. Registration: 3004972304 View Registration
CAIRE INC. Registration: 3009128734 View Registration
DEHAS Medical Systems GmbH Registration: 3013156250 View Registration

Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.