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FDA 510(k)

PLACER MODEL 6232 STEERABLE STYLET

K-Number: K000955 · 2000-06-16

ApplicantMedtronic Vascular
Decision Date2000-06-16
Product CodeDRB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PLACER MODEL 6232 STEERABLE STYLET is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2000-06-16 under 510(k) number K000955. The device is classified under product code DRB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLACER MODEL 6232 STEERABLE STYLET?

PLACER MODEL 6232 STEERABLE STYLET is a medical device that received FDA 510(k) clearance on 2000-06-16. The listed applicant is Medtronic Vascular. The 510(k) number is K000955.

When did PLACER MODEL 6232 STEERABLE STYLET receive FDA 510(k) clearance?

PLACER MODEL 6232 STEERABLE STYLET received FDA 510(k) clearance on 2000-06-16, under 510(k) number K000955.

Who is the listed applicant for PLACER MODEL 6232 STEERABLE STYLET?

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

What is the FDA product code for PLACER MODEL 6232 STEERABLE STYLET?

The FDA product code for PLACER MODEL 6232 STEERABLE STYLET is DRB.

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Other records listing Medtronic Vascular as applicant

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Related Devices (Code: DRB)

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.

K220280Arrow Stiffening StyletArrow International, LLC (A subsidiary of Teleflex, Inc.)K191469Biotronik StyletsBiotronik, Inc.K182660GaltTWSGalt Medical Corp.K170298Liberator Beacon Tip Locking StyletCook IncorporatedK090163STYLET, MODELS 4060, 4062, 4064, 4090, 4091 AND 4078St Jude MedicalK080924MOND RVOT STYLET MODELS 4140, 4141, 4150, 4151St. Jude Medical, Cardiac Rhythm Management Divisi

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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