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FDA 510(k)

STERILE CHEST TUBE

K-Number: K913733 · 1991-10-08

ApplicantVascular Products, Inc.
Decision Date1991-10-08
Product CodeGBW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE CHEST TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Products, Inc.. It received FDA 510(k) clearance on 1991-10-08 under 510(k) number K913733. The device is classified under product code GBW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE CHEST TUBE?

STERILE CHEST TUBE is a medical device that received FDA 510(k) clearance on 1991-10-08. The listed applicant is Vascular Products, Inc.. The 510(k) number is K913733.

When did STERILE CHEST TUBE receive FDA 510(k) clearance?

STERILE CHEST TUBE received FDA 510(k) clearance on 1991-10-08, under 510(k) number K913733.

Who is the listed applicant for STERILE CHEST TUBE?

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

What is the FDA product code for STERILE CHEST TUBE?

The FDA product code for STERILE CHEST TUBE is GBW.

Related Clinical Trials

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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Other records listing Vascular Products, 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.

K910840VASCULAR BIOPSY FORCEPSK823447IMPLANTABLE PACING LEAD, TINED #3262 &

Related Devices (Code: GBW)

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.

K992907INTRADUCERTaut, Inc.K992904MINI-PORTTaut, Inc.K972112INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450Taut, Inc.K961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAINSil-Med Corp.K960426MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETERMedical Components, Inc.K942709MEDIASTINAL SILICONE DRAINSSil-Med Corp.

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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