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FDA 510(k)

TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR

K-Number: K934348 · 1994-12-23

ApplicantTri-Med Specialties, Inc.
Decision Date1994-12-23
Product CodeBSS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med Specialties, Inc.. It received FDA 510(k) clearance on 1994-12-23 under 510(k) number K934348. The device is classified under product code BSS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR?

TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR is a medical device that received FDA 510(k) clearance on 1994-12-23. The listed applicant is Tri-Med Specialties, Inc.. The 510(k) number is K934348.

When did TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR receive FDA 510(k) clearance?

TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR received FDA 510(k) clearance on 1994-12-23, under 510(k) number K934348.

Who is the listed applicant for TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR?

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

What is the FDA product code for TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR?

The FDA product code for TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR is BSS.

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Other records listing Tri-Med Specialties, 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.

K971615PATTISON ESOPHAGEAL DILATORK970890#ES-32 SUCTION CATHETER 32 FR.K970982T-RX RETRIEVAL FORCEPSK942918TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETERK950574NEEDLE/CANNULAK945160PARACENTESIS NEEDLES/CANNULAS

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Related Devices (Code: BSS)

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.

K051480ENTERAL FEEDING TUBEBiosearch Medical Products, Inc.K984629MOSS TUBES, INC. NASAL TUBE - MARK IVMoss Tubes, Inc.K961711ASPISAFE GASTRIC TUBEB.Braun Medical, Inc.K933596GASTRIC, CATHETER, IRRIGATION & ASPIRATIONPolamedco, Inc.K930510RADIUS ENTERAL FEEDING TUBERadius Intl., Inc.K935688AN-10S ANDERSEN TUBE WITH STYLETH.W. Andersen Products, 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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