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FDA 510(k)

IMPLANT PARALLELING DEVICE (I.P.D.)

K-Number: K890433 · 1989-06-16

Decision Date1989-06-16
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLANT PARALLELING DEVICE (I.P.D.) is the device name listed in this FDA 510(k) record. The listed applicant is J.E. Josephson, D.M.D.. It received FDA 510(k) clearance on 1989-06-16 under 510(k) number K890433. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANT PARALLELING DEVICE (I.P.D.)?

IMPLANT PARALLELING DEVICE (I.P.D.) is a medical device that received FDA 510(k) clearance on 1989-06-16. The listed applicant is J.E. Josephson, D.M.D.. The 510(k) number is K890433.

When did IMPLANT PARALLELING DEVICE (I.P.D.) receive FDA 510(k) clearance?

IMPLANT PARALLELING DEVICE (I.P.D.) received FDA 510(k) clearance on 1989-06-16, under 510(k) number K890433.

Who is the listed applicant for IMPLANT PARALLELING DEVICE (I.P.D.)?

The FDA 510(k) record lists J.E. Josephson, D.M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLANT PARALLELING DEVICE (I.P.D.)?

The FDA product code for IMPLANT PARALLELING DEVICE (I.P.D.) is EFB.

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.

Related Devices (Code: EFB)

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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