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FDA 510(k)

JENKER NEEDLE STICK PROTECTOR

K-Number: K920758 · 1992-04-28

Decision Date1992-04-28
Product CodeDZM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JENKER NEEDLE STICK PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1992-04-28 under 510(k) number K920758. The device is classified under product code DZM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JENKER NEEDLE STICK PROTECTOR?

JENKER NEEDLE STICK PROTECTOR is a medical device that received FDA 510(k) clearance on 1992-04-28. The listed applicant is Dentsply Intl.. The 510(k) number is K920758.

When did JENKER NEEDLE STICK PROTECTOR receive FDA 510(k) clearance?

JENKER NEEDLE STICK PROTECTOR received FDA 510(k) clearance on 1992-04-28, under 510(k) number K920758.

Who is the listed applicant for JENKER NEEDLE STICK PROTECTOR?

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

What is the FDA product code for JENKER NEEDLE STICK PROTECTOR?

The FDA product code for JENKER NEEDLE STICK PROTECTOR is DZM.

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 Dentsply Intl. 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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Related Devices (Code: DZM)

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.

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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