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FDA 510(k)

CONTAIN-OR

K-Number: K934215 · 1994-02-09

ApplicantDlp, Inc.
Decision Date1994-02-09
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONTAIN-OR is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K934215. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 56 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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