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FDA 510(k)

MACRO SUCTION TUBE MODEL NO 10061

K-Number: K950754 · 1995-04-25

ApplicantDlp, Inc.
Decision Date1995-04-25
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MACRO SUCTION TUBE MODEL NO 10061 is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1995-04-25 under 510(k) number K950754. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MACRO SUCTION TUBE MODEL NO 10061?

MACRO SUCTION TUBE MODEL NO 10061 is a medical device that received FDA 510(k) clearance on 1995-04-25. The listed applicant is Dlp, Inc.. The 510(k) number is K950754.

When did MACRO SUCTION TUBE MODEL NO 10061 receive FDA 510(k) clearance?

MACRO SUCTION TUBE MODEL NO 10061 received FDA 510(k) clearance on 1995-04-25, under 510(k) number K950754.

Who is the listed applicant for MACRO SUCTION TUBE MODEL NO 10061?

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 MACRO SUCTION TUBE MODEL NO 10061?

The FDA product code for MACRO SUCTION TUBE MODEL NO 10061 is GCY.

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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 STYLETK934215CONTAIN-ORK915268CATHETER TWO STAGE VENOUS RETURNK914608BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120

View all 56 devices →

Related Devices (Code: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.K930615AUTOVAC CLOSED WOUND SUCTION SYSTEMBoehringer Laboratories

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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