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FDA 510(k)

PDI PARALLEL SIDED POST KIT

K-Number: K913019 · 1991-10-02

ApplicantPrecident Corp.
Decision Date1991-10-02
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PDI PARALLEL SIDED POST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Precident Corp.. It received FDA 510(k) clearance on 1991-10-02 under 510(k) number K913019. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PDI PARALLEL SIDED POST KIT?

PDI PARALLEL SIDED POST KIT is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is Precident Corp.. The 510(k) number is K913019.

When did PDI PARALLEL SIDED POST KIT receive FDA 510(k) clearance?

PDI PARALLEL SIDED POST KIT received FDA 510(k) clearance on 1991-10-02, under 510(k) number K913019.

Who is the listed applicant for PDI PARALLEL SIDED POST KIT?

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

What is the FDA product code for PDI PARALLEL SIDED POST KIT?

The FDA product code for PDI PARALLEL SIDED POST KIT is ELR.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Precident 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.

K911323FLUX-N-ALL

Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.

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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