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FDA 510(k)

NEBULIZER, MOLEL 503, PART #17068

K-Number: K771105 · 1977-07-05

ApplicantHospal Medical Corp.
Decision Date1977-07-05
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER, MOLEL 503, PART #17068 is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1977-07-05 under 510(k) number K771105. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEBULIZER, MOLEL 503, PART #17068?

NEBULIZER, MOLEL 503, PART #17068 is a medical device that received FDA 510(k) clearance on 1977-07-05. The listed applicant is Hospal Medical Corp.. The 510(k) number is K771105.

When did NEBULIZER, MOLEL 503, PART #17068 receive FDA 510(k) clearance?

NEBULIZER, MOLEL 503, PART #17068 received FDA 510(k) clearance on 1977-07-05, under 510(k) number K771105.

Who is the listed applicant for NEBULIZER, MOLEL 503, PART #17068?

The FDA 510(k) record lists Hospal Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEBULIZER, MOLEL 503, PART #17068?

The FDA product code for NEBULIZER, MOLEL 503, PART #17068 is CAF.

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Related Devices (Code: CAF)

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.

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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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