36-101 XDS111 XENON DELIVERY/TRAP SYSTEM
K-Number: K860504 · 1986-04-04
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Device Summary
Frequently Asked Questions
What is the 36-101 XDS111 XENON DELIVERY/TRAP SYSTEM?
36-101 XDS111 XENON DELIVERY/TRAP SYSTEM is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Victoreen, Inc.. The 510(k) number is K860504.
When did 36-101 XDS111 XENON DELIVERY/TRAP SYSTEM receive FDA 510(k) clearance?
36-101 XDS111 XENON DELIVERY/TRAP SYSTEM received FDA 510(k) clearance on 1986-04-04, under 510(k) number K860504.
Who is the listed applicant for 36-101 XDS111 XENON DELIVERY/TRAP SYSTEM?
The FDA 510(k) record lists Victoreen, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 36-101 XDS111 XENON DELIVERY/TRAP SYSTEM?
The FDA product code for 36-101 XDS111 XENON DELIVERY/TRAP SYSTEM is ITY.
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 Victoreen, 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: ITY)
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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