Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDIUM CONCENTRATION OXYGEN MASKS

K-Number: K860869 · 1986-03-19

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

Device Summary

MEDIUM CONCENTRATION OXYGEN MASKS 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 K860869. 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 MEDIUM CONCENTRATION OXYGEN MASKS?

MEDIUM CONCENTRATION OXYGEN MASKS 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 K860869.

When did MEDIUM CONCENTRATION OXYGEN MASKS receive FDA 510(k) clearance?

MEDIUM CONCENTRATION OXYGEN MASKS received FDA 510(k) clearance on 1986-03-19, under 510(k) number K860869.

Who is the listed applicant for MEDIUM CONCENTRATION OXYGEN MASKS?

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 MEDIUM CONCENTRATION OXYGEN MASKS?

The FDA product code for MEDIUM CONCENTRATION OXYGEN MASKS 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

View on FDA Database →

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

↑