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FDA 510(k)

SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE

K-Number: K770642 · 1977-04-15

Decision Date1977-04-15
Product CodeEIC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770642. The device is classified under product code EIC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE?

SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is National Patent Development Corp.. The 510(k) number is K770642.

When did SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE receive FDA 510(k) clearance?

SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770642.

Who is the listed applicant for SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE?

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

What is the FDA product code for SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE?

The FDA product code for SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLE is EIC.

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 National Patent Development Corp. 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 34 devices →

Related Devices (Code: EIC)

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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