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FDA 510(k)

SEARE BIOMEDICAL CHIN IMPLANTS

K-Number: K982752 · 1998-09-30

ApplicantSeare Biomedical Corp.
Decision Date1998-09-30
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEARE BIOMEDICAL CHIN IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Seare Biomedical Corp.. It received FDA 510(k) clearance on 1998-09-30 under 510(k) number K982752. The device is classified under product code FWP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEARE BIOMEDICAL CHIN IMPLANTS?

SEARE BIOMEDICAL CHIN IMPLANTS is a medical device that received FDA 510(k) clearance on 1998-09-30. The listed applicant is Seare Biomedical Corp.. The 510(k) number is K982752.

When did SEARE BIOMEDICAL CHIN IMPLANTS receive FDA 510(k) clearance?

SEARE BIOMEDICAL CHIN IMPLANTS received FDA 510(k) clearance on 1998-09-30, under 510(k) number K982752.

Who is the listed applicant for SEARE BIOMEDICAL CHIN IMPLANTS?

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

What is the FDA product code for SEARE BIOMEDICAL CHIN IMPLANTS?

The FDA product code for SEARE BIOMEDICAL CHIN IMPLANTS is FWP.

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Other records listing Seare Biomedical 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.

K983792SEARE BIOMEDICAL SILICONE TISSUE EXPANDERK983630SEARE BIOMEDICAL SILICONE RODSK982753SEARE BIOMEDICAL NASAL IMPLANTSK982763SEARE BIOMEDICAL MALAR IMPLANTSK983043SEARE BIOMEDICAL SILICONE BLOCKK982762SEARE BIOMEDICAL PECTORALIS IMPLANT

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Related Devices (Code: FWP)

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.

K254233MEDPOR Customized Implant KitStryker Leibinger GmbH & Co KGK232593FITme Customized Silicone ImplantKeosan Trading Co.K200610Customized Contour ImplantImplantech Associates, Inc.K191130Customized Contour ImplantImplantech Associates, Inc.K191916Stryker CMF MEDPOR Priority Customized Implant KitStryker Leibinger GmbH & Co KGK153508Stryker CMF MEDPOR Customized ImplantStryker

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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