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FDA 510(k)

LIQUID OXYGEN STORAGE SUBSYSTEM

K-Number: K941819 · 1994-05-23

ApplicantHogan & Hartson
Decision Date1994-05-23
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIQUID OXYGEN STORAGE SUBSYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1994-05-23 under 510(k) number K941819. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID OXYGEN STORAGE SUBSYSTEM?

LIQUID OXYGEN STORAGE SUBSYSTEM is a medical device that received FDA 510(k) clearance on 1994-05-23. The listed applicant is Hogan & Hartson. The 510(k) number is K941819.

When did LIQUID OXYGEN STORAGE SUBSYSTEM receive FDA 510(k) clearance?

LIQUID OXYGEN STORAGE SUBSYSTEM received FDA 510(k) clearance on 1994-05-23, under 510(k) number K941819.

Who is the listed applicant for LIQUID OXYGEN STORAGE SUBSYSTEM?

The FDA 510(k) record lists Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUID OXYGEN STORAGE SUBSYSTEM?

The FDA product code for LIQUID OXYGEN STORAGE SUBSYSTEM is BYJ.

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Other records listing Hogan & Hartson as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K974168COOPERSURGICAL INFRARED COAGULATORK973849BIOABSORBABLE BANKART TACKK973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEK950169RIBOSOMAL P EIA TEST SYSTEMK942389TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVESK946217CARDIOLIPIN M EIA TEST SYSTEM

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Related Devices (Code: BYJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K130068DISMOUNTED MEDICAL & SUPPLEMENTAL OXYGEN SYSTEM (DMOS)Essex Industries, Inc. D/B/A Essex Cryogenics of MK113767MOUNTED MEDICAL OXYGEN SYSTEMEssex Industries, Inc.K103324PRECISION LIQUID OXYGEN SYSTEMPrecision Medical, Inc.K101272MASS OXYGEN DISTRIBUTION SYSTEM (MODS) MODEL 10C-0061-3Essex Industries, Inc.K081779GOLOX-93Respironics, Inc.K080023MODIFICATION TO: SPIRITCaire, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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