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FDA 510(k)

AEROSOL MASKS/ADULT & PAEDIATRIC

K-Number: K860870 · 1986-03-19

Decision Date1986-03-19
Product CodeBYG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AEROSOL MASKS/ADULT & PAEDIATRIC 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 1986-03-19 under 510(k) number K860870. The device is classified under product code BYG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROSOL MASKS/ADULT & PAEDIATRIC?

AEROSOL MASKS/ADULT & PAEDIATRIC is a medical device that received FDA 510(k) clearance on 1986-03-19. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K860870.

When did AEROSOL MASKS/ADULT & PAEDIATRIC receive FDA 510(k) clearance?

AEROSOL MASKS/ADULT & PAEDIATRIC received FDA 510(k) clearance on 1986-03-19, under 510(k) number K860870.

Who is the listed applicant for AEROSOL MASKS/ADULT & PAEDIATRIC?

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 AEROSOL MASKS/ADULT & PAEDIATRIC?

The FDA product code for AEROSOL MASKS/ADULT & PAEDIATRIC is BYG.

Related Clinical Trials

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.

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.

View all 43 devices →

Related Devices (Code: BYG)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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