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)

L-3 PURGE LINE

K-Number: K802602 · 1980-11-12

Decision Date1980-11-12
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

L-3 PURGE LINE is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Industries. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802602. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L-3 PURGE LINE?

L-3 PURGE LINE is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Delta Medical Industries. The 510(k) number is K802602.

When did L-3 PURGE LINE receive FDA 510(k) clearance?

L-3 PURGE LINE received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802602.

Who is the listed applicant for L-3 PURGE LINE?

The FDA 510(k) record lists Delta Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-3 PURGE LINE?

The FDA product code for L-3 PURGE LINE is DTM.

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 Delta Medical Industries 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 27 devices →

Related Devices (Code: DTM)

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.

↑