L-3 PURGE LINE
K-Number: K802602 · 1980-11-12
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Device Summary
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.
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.
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