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FDA 510(k)

INTRADUCER

K-Number: K992907 · 1999-10-05

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

Device Summary

INTRADUCER 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 K992907. 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 INTRADUCER?

INTRADUCER 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 K992907.

When did INTRADUCER receive FDA 510(k) clearance?

INTRADUCER received FDA 510(k) clearance on 1999-10-05, under 510(k) number K992907.

Who is the listed applicant for INTRADUCER?

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 INTRADUCER?

The FDA product code for INTRADUCER is GBW.

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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 NEEDLEK992904MINI-PORT

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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.

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.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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