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FDA 510(k)

AD POST

K-Number: K884277 · 1988-12-22

ApplicantJ. Morita USA, Inc.
Decision Date1988-12-22
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AD POST is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 1988-12-22 under 510(k) number K884277. 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 AD POST?

AD POST is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K884277.

When did AD POST receive FDA 510(k) clearance?

AD POST received FDA 510(k) clearance on 1988-12-22, under 510(k) number K884277.

Who is the listed applicant for AD POST?

The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AD POST?

The FDA product code for AD POST is ELR.

Related PubMed Literature

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.

PMID: 39720009Validation and Final Results from the First Cardiac Lead Post-Approval Study Using Real-World Data.Pragmatic and observational research ()

Other records listing J. Morita USA, Inc. 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.

K213477Root ZX3K2013783D Accuitomo 150NK190509Lubrina 2K173920LS OILK171012Veraview X800K170275Tri Auto ZX2

View all 52 devices →

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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