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FDA 510(k)

CATHETER TWO STAGE VENOUS RETURN

K-Number: K915268 · 1992-07-27

ApplicantDlp, Inc.
Decision Date1992-07-27
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHETER TWO STAGE VENOUS RETURN is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1992-07-27 under 510(k) number K915268. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER TWO STAGE VENOUS RETURN?

CATHETER TWO STAGE VENOUS RETURN is a medical device that received FDA 510(k) clearance on 1992-07-27. The listed applicant is Dlp, Inc.. The 510(k) number is K915268.

When did CATHETER TWO STAGE VENOUS RETURN receive FDA 510(k) clearance?

CATHETER TWO STAGE VENOUS RETURN received FDA 510(k) clearance on 1992-07-27, under 510(k) number K915268.

Who is the listed applicant for CATHETER TWO STAGE VENOUS RETURN?

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 CATHETER TWO STAGE VENOUS RETURN?

The FDA product code for CATHETER TWO STAGE VENOUS RETURN is DWF.

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Other records listing Dlp, Inc. as applicant

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Related Devices (Code: DWF)

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.

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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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