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FDA 510(k)

ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE

K-Number: K926073 · 1995-05-15

ApplicantSurgimark, Inc.
Decision Date1995-05-15
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Surgimark, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K926073. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE?

ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Surgimark, Inc.. The 510(k) number is K926073.

When did ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE receive FDA 510(k) clearance?

ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE received FDA 510(k) clearance on 1995-05-15, under 510(k) number K926073.

Who is the listed applicant for ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE?

The FDA 510(k) record lists Surgimark, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE?

The FDA product code for ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE is FEG.

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Other records listing Surgimark, 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.

K932689LAPRO-LOADER(TM)K871950VIA-GUARD

Related Devices (Code: FEG)

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.

K17161914Fr Colon Decompression Set, Macon Colon Decompression SetCook Ireland, Ltd.K132314MEDLINE ANTI-REFLUX VALVEMedline Industries, Inc.K053410GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTORKendallK040388NEXT GENERATION SALEM SUMPKendallK971354KNOTT NG TUBEMichael M. Knott, M.D.K960176DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTERC.R. Bard, Inc.

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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