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FDA 510(k)

DISPOSSABLE SUCTION TUBE, 6 FRENCH

K-Number: K791846 · 1979-10-02

ApplicantDlp, Inc.
Decision Date1979-10-02
Product CodeDTS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSSABLE SUCTION TUBE, 6 FRENCH is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1979-10-02 under 510(k) number K791846. The device is classified under product code DTS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSSABLE SUCTION TUBE, 6 FRENCH?

DISPOSSABLE SUCTION TUBE, 6 FRENCH is a medical device that received FDA 510(k) clearance on 1979-10-02. The listed applicant is Dlp, Inc.. The 510(k) number is K791846.

When did DISPOSSABLE SUCTION TUBE, 6 FRENCH receive FDA 510(k) clearance?

DISPOSSABLE SUCTION TUBE, 6 FRENCH received FDA 510(k) clearance on 1979-10-02, under 510(k) number K791846.

Who is the listed applicant for DISPOSSABLE SUCTION TUBE, 6 FRENCH?

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 DISPOSSABLE SUCTION TUBE, 6 FRENCH?

The FDA product code for DISPOSSABLE SUCTION TUBE, 6 FRENCH is DTS.

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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.

K973485CLEARVIEW BLOWER/MISTERK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)K953945RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLETK950754MACRO SUCTION TUBE MODEL NO 10061K934215CONTAIN-ORK915268CATHETER TWO STAGE VENOUS RETURN

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Related Devices (Code: DTS)

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.

K053021ESTECH CLEARVIEW MV ATRIAL DEPRESSOREstech, Inc.K982891CALIFORNIA MEDICAL LABORATORIES INC. STANDARD AND SMALL RIGID TIP SUCTION WANDSCalifornia Medical Laboratories, Inc.K963756IBC CARDIAC SUCTION WARDInternational Biophysics Corp.K905008FLEXIBLE INTRACARDIAC SUCTION DEVICEGish Biomedical, Inc.K900339HAND-HELD INTRACARDIAC SUCKERS W/ERGONOMIC HANDLESShiley, Inc.K891906ROBICSEK INTRACARDIAC SUCTION WANDGish Biomedical, Inc.

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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