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FDA 510(k)

RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR

K-Number: K853083 · 1985-09-03

ApplicantHome Medical Supply, Inc.
Decision Date1985-09-03
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR is the device name listed in this FDA 510(k) record. The listed applicant is Home Medical Supply, Inc.. It received FDA 510(k) clearance on 1985-09-03 under 510(k) number K853083. 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 RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR?

RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR is a medical device that received FDA 510(k) clearance on 1985-09-03. The listed applicant is Home Medical Supply, Inc.. The 510(k) number is K853083.

When did RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR receive FDA 510(k) clearance?

RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR received FDA 510(k) clearance on 1985-09-03, under 510(k) number K853083.

Who is the listed applicant for RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR?

The FDA 510(k) record lists Home Medical Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR?

The FDA product code for RESERVIOR-MASTERAIR PORTABLE-FREEDOMAIR is BYJ.

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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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