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FDA 510(k)

VASCATH VASCULAR CATHETER PLACEMENT KIT

K-Number: K870542 · 1987-04-27

ApplicantTitan Medical, Inc.
Decision Date1987-04-27
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCATH VASCULAR CATHETER PLACEMENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Titan Medical, Inc.. It received FDA 510(k) clearance on 1987-04-27 under 510(k) number K870542. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCATH VASCULAR CATHETER PLACEMENT KIT?

VASCATH VASCULAR CATHETER PLACEMENT KIT is a medical device that received FDA 510(k) clearance on 1987-04-27. The listed applicant is Titan Medical, Inc.. The 510(k) number is K870542.

When did VASCATH VASCULAR CATHETER PLACEMENT KIT receive FDA 510(k) clearance?

VASCATH VASCULAR CATHETER PLACEMENT KIT received FDA 510(k) clearance on 1987-04-27, under 510(k) number K870542.

Who is the listed applicant for VASCATH VASCULAR CATHETER PLACEMENT KIT?

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

What is the FDA product code for VASCATH VASCULAR CATHETER PLACEMENT KIT?

The FDA product code for VASCATH VASCULAR CATHETER PLACEMENT KIT is DYB.

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 Titan Medical, 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.

K875213SURECATH - ITP II PERCUTANEOUS PORT ACCESS DEVICEK872149SURECATH-ITP PERCUTANEOUS ACCESS KIT

Related Devices (Code: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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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