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FDA 510(k)

NEBULIZER NO. M-175

K-Number: K790924 · 1979-05-21

ApplicantMem Medical, Inc.
Decision Date1979-05-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER NO. M-175 is the device name listed in this FDA 510(k) record. The listed applicant is Mem Medical, Inc.. It received FDA 510(k) clearance on 1979-05-21 under 510(k) number K790924. 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 NO. M-175?

NEBULIZER NO. M-175 is a medical device that received FDA 510(k) clearance on 1979-05-21. The listed applicant is Mem Medical, Inc.. The 510(k) number is K790924.

When did NEBULIZER NO. M-175 receive FDA 510(k) clearance?

NEBULIZER NO. M-175 received FDA 510(k) clearance on 1979-05-21, under 510(k) number K790924.

Who is the listed applicant for NEBULIZER NO. M-175?

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

What is the FDA product code for NEBULIZER NO. M-175?

The FDA product code for NEBULIZER NO. M-175 is CAF.

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Other records listing Mem Medical, 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.

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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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