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FDA 510(k)

MANIFOLD/NEBULIZER BREATHING PRODUCTS

K-Number: K791469 · 1979-08-28

ApplicantHospitak, Inc.
Decision Date1979-08-28
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MANIFOLD/NEBULIZER BREATHING PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1979-08-28 under 510(k) number K791469. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANIFOLD/NEBULIZER BREATHING PRODUCTS?

MANIFOLD/NEBULIZER BREATHING PRODUCTS is a medical device that received FDA 510(k) clearance on 1979-08-28. The listed applicant is Hospitak, Inc.. The 510(k) number is K791469.

When did MANIFOLD/NEBULIZER BREATHING PRODUCTS receive FDA 510(k) clearance?

MANIFOLD/NEBULIZER BREATHING PRODUCTS received FDA 510(k) clearance on 1979-08-28, under 510(k) number K791469.

Who is the listed applicant for MANIFOLD/NEBULIZER BREATHING PRODUCTS?

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 MANIFOLD/NEBULIZER BREATHING PRODUCTS?

The FDA product code for MANIFOLD/NEBULIZER BREATHING PRODUCTS is BZO.

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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)K954787ILLUMINATORK953620WARM N WET HMEF W/LUER ADAPTERK953619WARM N WET HME W/LUER ADAPTERK915750DISPOSABLE BACTERIAL BREATHNG FILTERK920842AEROSOL DELIVERY SYSTEMS

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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