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FDA 510(k)

NEBULIZER, MEDICINAL

K-Number: K802430 · 1980-10-23

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1980-10-23
Product CodeEPN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER, MEDICINAL is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802430. The device is classified under product code EPN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEBULIZER, MEDICINAL?

NEBULIZER, MEDICINAL is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K802430.

When did NEBULIZER, MEDICINAL receive FDA 510(k) clearance?

NEBULIZER, MEDICINAL received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802430.

Who is the listed applicant for NEBULIZER, MEDICINAL?

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

What is the FDA product code for NEBULIZER, MEDICINAL?

The FDA product code for NEBULIZER, MEDICINAL is EPN.

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Other records listing Dhd Medical Products Div. Diemolding Corp. 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.

K883988NON-REBREATHING TEE PIECE (NRTP)K881935MICROCIRRUS MEDICAL NEBULIZERK881178CUFFCHECKK873498INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBINGK874047ASTHMAKITK873447DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR

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Related Devices (Code: EPN)

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.

K896090DEVILBISS MODEL 6300DDevilbiss Health Care, 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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