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)

MOISTURE TRAP

K-Number: K820936 · 1982-04-29

Decision Date1982-04-29
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOISTURE TRAP 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 1982-04-29 under 510(k) number K820936. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOISTURE TRAP?

MOISTURE TRAP is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K820936.

When did MOISTURE TRAP receive FDA 510(k) clearance?

MOISTURE TRAP received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820936.

Who is the listed applicant for MOISTURE TRAP?

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 MOISTURE TRAP?

The FDA product code for MOISTURE TRAP is BYH.

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: BYH)

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.

↑