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FDA 510(k)

AEROSOL DELIVERY SYSTEMS

K-Number: K920842 · 1992-05-15

ApplicantHospitak, Inc.
Decision Date1992-05-15
Product CodeLRD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AEROSOL DELIVERY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1992-05-15 under 510(k) number K920842. The device is classified under product code LRD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROSOL DELIVERY SYSTEMS?

AEROSOL DELIVERY SYSTEMS is a medical device that received FDA 510(k) clearance on 1992-05-15. The listed applicant is Hospitak, Inc.. The 510(k) number is K920842.

When did AEROSOL DELIVERY SYSTEMS receive FDA 510(k) clearance?

AEROSOL DELIVERY SYSTEMS received FDA 510(k) clearance on 1992-05-15, under 510(k) number K920842.

Who is the listed applicant for AEROSOL DELIVERY SYSTEMS?

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

What is the FDA product code for AEROSOL DELIVERY SYSTEMS?

The FDA product code for AEROSOL DELIVERY SYSTEMS is LRD.

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Other records listing Hospitak, Inc. 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.

K955483TRACH MASK MODEL (245, 246)K954787ILLUMINATORK953619WARM N WET HME W/LUER ADAPTERK953620WARM N WET HMEF W/LUER ADAPTERK915750DISPOSABLE BACTERIAL BREATHNG FILTERK915228DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL

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Related Devices (Code: LRD)

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.

K984345AROMAPATCHEnvis, Inc.K932522AMSCO STERILE RECOVERIES SURGICAL PACKSAmsco Sterile Recoveries, Inc.K942789MISTASSISTThe Merlin Corp.K940133THE EXPANDACELL EAR PACKDenver Splint Co.K925022SURGICAL TRAY (STERILE)Customed, 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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