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FDA 510(k)

REINFORCING PIN

K-Number: K822412 · 1982-08-30

ApplicantFilhol
Decision Date1982-08-30
Product CodeEBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REINFORCING PIN is the device name listed in this FDA 510(k) record. The listed applicant is Filhol. It received FDA 510(k) clearance on 1982-08-30 under 510(k) number K822412. The device is classified under product code EBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REINFORCING PIN?

REINFORCING PIN is a medical device that received FDA 510(k) clearance on 1982-08-30. The listed applicant is Filhol. The 510(k) number is K822412.

When did REINFORCING PIN receive FDA 510(k) clearance?

REINFORCING PIN received FDA 510(k) clearance on 1982-08-30, under 510(k) number K822412.

Who is the listed applicant for REINFORCING PIN?

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

What is the FDA product code for REINFORCING PIN?

The FDA product code for REINFORCING PIN is EBL.

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Related Devices (Code: EBL)

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.

K002693CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)Cbs Intl. B.V.K952868DENTAURUM JACKET CROWN & ROOT POSTSDentauraum, Inc.K924376ROOT CANAL POSTThe Thera GroupK895283PROSTHETIC RESTORATION DEVICESwiss Precision Mfg. Corp.K895758PLASTIC TOOTH REINFORCEMENT KITNanzee Dental ProductsK883074ELGILOYDale T. Dupuis

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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