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FDA 510(k)

1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS

K-Number: K851719 · 1985-07-02

ApplicantArtiberia
Decision Date1985-07-02
Product CodeEZZ
DecisionSubstantially Equivalent

Device Summary

1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K851719. The device is classified under product code EZZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS?

1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Artiberia. The 510(k) number is K851719.

When did 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS receive FDA 510(k) clearance?

1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851719.

Who is the listed applicant for 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS?

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

What is the FDA product code for 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS?

The FDA product code for 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS is EZZ.

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.

Other records listing Artiberia 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.

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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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