CONTAIN-OR
K-Number: K934215 · 1994-02-09
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Device Summary
Frequently Asked Questions
What is the CONTAIN-OR?
CONTAIN-OR is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Dlp, Inc.. The 510(k) number is K934215.
When did CONTAIN-OR receive FDA 510(k) clearance?
CONTAIN-OR received FDA 510(k) clearance on 1994-02-09, under 510(k) number K934215.
Who is the listed applicant for CONTAIN-OR?
The FDA 510(k) record lists Dlp, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTAIN-OR?
The FDA product code for CONTAIN-OR is KKX.
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 Dlp, 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: KKX)
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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