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)

SELF-SEALING WATER TRAP/ACCESSORIES

K-Number: K860884 · 1986-03-19

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

Device Summary

SELF-SEALING WATER TRAP/ACCESSORIES 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 K860884. 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 SELF-SEALING WATER TRAP/ACCESSORIES?

SELF-SEALING WATER TRAP/ACCESSORIES 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 K860884.

When did SELF-SEALING WATER TRAP/ACCESSORIES receive FDA 510(k) clearance?

SELF-SEALING WATER TRAP/ACCESSORIES received FDA 510(k) clearance on 1986-03-19, under 510(k) number K860884.

Who is the listed applicant for SELF-SEALING WATER TRAP/ACCESSORIES?

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 SELF-SEALING WATER TRAP/ACCESSORIES?

The FDA product code for SELF-SEALING WATER TRAP/ACCESSORIES 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.

↑