CONTAIN(TM) LASER PLUME FILTER
K-Number: K902167 · 1991-01-04
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Device Summary
Frequently Asked Questions
What is the CONTAIN(TM) LASER PLUME FILTER?
CONTAIN(TM) LASER PLUME FILTER is a medical device that received FDA 510(k) clearance on 1991-01-04. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K902167.
When did CONTAIN(TM) LASER PLUME FILTER receive FDA 510(k) clearance?
CONTAIN(TM) LASER PLUME FILTER received FDA 510(k) clearance on 1991-01-04, under 510(k) number K902167.
Who is the listed applicant for CONTAIN(TM) LASER PLUME FILTER?
The FDA 510(k) record lists Arbor Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTAIN(TM) LASER PLUME FILTER?
The FDA product code for CONTAIN(TM) LASER PLUME FILTER is JDY.
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 Arbor Technologies, 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: JDY)
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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