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FDA 510(k)

MINI-PORT

K-Number: K992904 · 1999-10-05

ApplicantTaut, Inc.
Decision Date1999-10-05
Product CodeGBW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINI-PORT is the device name listed in this FDA 510(k) record. The listed applicant is Taut, Inc.. It received FDA 510(k) clearance on 1999-10-05 under 510(k) number K992904. 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 MINI-PORT?

MINI-PORT is a medical device that received FDA 510(k) clearance on 1999-10-05. The listed applicant is Taut, Inc.. The 510(k) number is K992904.

When did MINI-PORT receive FDA 510(k) clearance?

MINI-PORT received FDA 510(k) clearance on 1999-10-05, under 510(k) number K992904.

Who is the listed applicant for MINI-PORT?

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

What is the FDA product code for MINI-PORT?

The FDA product code for MINI-PORT is GBW.

Other records listing Taut, 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.

K023261ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244K021731ADAPT OPEN ACCESS PORT, MODEL 41233K011018TAUT BALLOON CATHETER, MODEL 50640K010007ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAPK003703TAUT-INSUFFLATION NEEDLEK992907INTRADUCER

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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.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.K933510ARGYLE TURKEL SAFETY TROCAR THORACIC CATHETERSherwood Medical Co.

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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