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FDA 510(k)

SAFETY PLUS DENTAL INJECTION NEEDLE

K-Number: K913573 · 1991-11-07

Decision Date1991-11-07
Product CodeDZM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SAFETY PLUS DENTAL INJECTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Specialites Septodont. It received FDA 510(k) clearance on 1991-11-07 under 510(k) number K913573. 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 SAFETY PLUS DENTAL INJECTION NEEDLE?

SAFETY PLUS DENTAL INJECTION NEEDLE is a medical device that received FDA 510(k) clearance on 1991-11-07. The listed applicant is Specialites Septodont. The 510(k) number is K913573.

When did SAFETY PLUS DENTAL INJECTION NEEDLE receive FDA 510(k) clearance?

SAFETY PLUS DENTAL INJECTION NEEDLE received FDA 510(k) clearance on 1991-11-07, under 510(k) number K913573.

Who is the listed applicant for SAFETY PLUS DENTAL INJECTION NEEDLE?

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

What is the FDA product code for SAFETY PLUS DENTAL INJECTION NEEDLE?

The FDA product code for SAFETY PLUS DENTAL INJECTION NEEDLE 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 Specialites Septodont 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.

View all 21 devices →

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

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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