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)

DALE ENDOTRACHEAL TUBE HOLDER

K-Number: K832946 · 1983-10-14

Decision Date1983-10-14
Product CodeJAY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DALE ENDOTRACHEAL TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Dale Medical Products, Inc.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832946. The device is classified under product code JAY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DALE ENDOTRACHEAL TUBE HOLDER?

DALE ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Dale Medical Products, Inc.. The 510(k) number is K832946.

When did DALE ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?

DALE ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832946.

Who is the listed applicant for DALE ENDOTRACHEAL TUBE HOLDER?

The FDA 510(k) record lists Dale Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DALE ENDOTRACHEAL TUBE HOLDER?

The FDA product code for DALE ENDOTRACHEAL TUBE HOLDER is JAY.

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 Dale Medical Products, Inc. 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 13 devices →

Related Devices (Code: JAY)

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.

↑