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FDA 510(k)

DIAL MEDICAL SUPPLY FISTULA NEEDLE SET

K-Number: K940441 · 1994-06-10

ApplicantDial Medical of Florida, Inc.
Decision Date1994-06-10
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIAL MEDICAL SUPPLY FISTULA NEEDLE SET is the device name listed in this FDA 510(k) record. The listed applicant is Dial Medical of Florida, Inc.. It received FDA 510(k) clearance on 1994-06-10 under 510(k) number K940441. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAL MEDICAL SUPPLY FISTULA NEEDLE SET?

DIAL MEDICAL SUPPLY FISTULA NEEDLE SET is a medical device that received FDA 510(k) clearance on 1994-06-10. The listed applicant is Dial Medical of Florida, Inc.. The 510(k) number is K940441.

When did DIAL MEDICAL SUPPLY FISTULA NEEDLE SET receive FDA 510(k) clearance?

DIAL MEDICAL SUPPLY FISTULA NEEDLE SET received FDA 510(k) clearance on 1994-06-10, under 510(k) number K940441.

Who is the listed applicant for DIAL MEDICAL SUPPLY FISTULA NEEDLE SET?

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

What is the FDA product code for DIAL MEDICAL SUPPLY FISTULA NEEDLE SET?

The FDA product code for DIAL MEDICAL SUPPLY FISTULA NEEDLE SET is FOZ.

Related Clinical Trials

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Other records listing Dial Medical of Florida, 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.

K864265HEMODIALYSIS BATH CONCENTRATE SOLUTIONS FOR HEMODI

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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