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)

DEANS DISPOSABLE T-TUBE INSERTER

K-Number: K924901 · 1993-01-28

Decision Date1993-01-28
Product CodeJYM
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DEANS DISPOSABLE T-TUBE INSERTER is the device name listed in this FDA 510(k) record. The listed applicant is Exmoor Plastics , Ltd.. It received FDA 510(k) clearance on 1993-01-28 under 510(k) number K924901. The device is classified under product code JYM. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEANS DISPOSABLE T-TUBE INSERTER?

DEANS DISPOSABLE T-TUBE INSERTER is a medical device that received FDA 510(k) clearance on 1993-01-28. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K924901.

When did DEANS DISPOSABLE T-TUBE INSERTER receive FDA 510(k) clearance?

DEANS DISPOSABLE T-TUBE INSERTER received FDA 510(k) clearance on 1993-01-28, under 510(k) number K924901.

Who is the listed applicant for DEANS DISPOSABLE T-TUBE INSERTER?

The FDA 510(k) record lists Exmoor Plastics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEANS DISPOSABLE T-TUBE INSERTER?

The FDA product code for DEANS DISPOSABLE T-TUBE INSERTER is JYM.

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 Exmoor Plastics , Ltd. 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: JYM)

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.

↑