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FDA 510(k)

STAGNONE SWIVEL-JOINT NEEDLE

K-Number: K861453 · 1986-05-06

ApplicantRadtech, Inc.
Decision Date1986-05-06
Product Code
DecisionSubstantially Equivalent

Device Summary

STAGNONE SWIVEL-JOINT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Radtech, Inc.. It received FDA 510(k) clearance on 1986-05-06 under 510(k) number K861453. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAGNONE SWIVEL-JOINT NEEDLE?

STAGNONE SWIVEL-JOINT NEEDLE is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Radtech, Inc.. The 510(k) number is K861453.

When did STAGNONE SWIVEL-JOINT NEEDLE receive FDA 510(k) clearance?

STAGNONE SWIVEL-JOINT NEEDLE received FDA 510(k) clearance on 1986-05-06, under 510(k) number K861453.

Who is the listed applicant for STAGNONE SWIVEL-JOINT NEEDLE?

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

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 Radtech, 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.

K860763RADTECH VASCULAR STENT

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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