DELTA TROL I & II
K-Number: K853373 · 1985-08-23
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Device Summary
Frequently Asked Questions
What is the DELTA TROL I & II?
DELTA TROL I & II is a medical device that received FDA 510(k) clearance on 1985-08-23. The listed applicant is Electro-Nucleonics Laboratories, Inc.. The 510(k) number is K853373.
When did DELTA TROL I & II receive FDA 510(k) clearance?
DELTA TROL I & II received FDA 510(k) clearance on 1985-08-23, under 510(k) number K853373.
Who is the listed applicant for DELTA TROL I & II?
The FDA 510(k) record lists Electro-Nucleonics Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DELTA TROL I & II?
The FDA product code for DELTA TROL I & II is JJT.
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 Electro-Nucleonics Laboratories, 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.
Related Devices (Code: JJT)
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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