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FDA 510(k)

BPOS-IVAD STABILIZER

K-Number: K983480 · 1998-11-23

ApplicantBpos, Inc.
Decision Date1998-11-23
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BPOS-IVAD STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Bpos, Inc.. It received FDA 510(k) clearance on 1998-11-23 under 510(k) number K983480. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BPOS-IVAD STABILIZER?

BPOS-IVAD STABILIZER is a medical device that received FDA 510(k) clearance on 1998-11-23. The listed applicant is Bpos, Inc.. The 510(k) number is K983480.

When did BPOS-IVAD STABILIZER receive FDA 510(k) clearance?

BPOS-IVAD STABILIZER received FDA 510(k) clearance on 1998-11-23, under 510(k) number K983480.

Who is the listed applicant for BPOS-IVAD STABILIZER?

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

What is the FDA product code for BPOS-IVAD STABILIZER?

The FDA product code for BPOS-IVAD STABILIZER is LJT.

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: LJT)

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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