Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MAGNET PAD

K-Number: K896802 · 1989-12-27

ApplicantWestmark, Sterile Packing Systems, Inc. (Sps)
Decision Date1989-12-27
Product CodeLXG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNET PAD is the device name listed in this FDA 510(k) record. The listed applicant is Westmark, Sterile Packing Systems, Inc. (Sps). It received FDA 510(k) clearance on 1989-12-27 under 510(k) number K896802. The device is classified under product code LXG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNET PAD?

MAGNET PAD is a medical device that received FDA 510(k) clearance on 1989-12-27. The listed applicant is Westmark, Sterile Packing Systems, Inc. (Sps). The 510(k) number is K896802.

When did MAGNET PAD receive FDA 510(k) clearance?

MAGNET PAD received FDA 510(k) clearance on 1989-12-27, under 510(k) number K896802.

Who is the listed applicant for MAGNET PAD?

The FDA 510(k) record lists Westmark, Sterile Packing Systems, Inc. (Sps) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNET PAD?

The FDA product code for MAGNET PAD is LXG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Westmark, Sterile Packing Systems, Inc. (Sps) 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.

K896800IRRIGATION TRAYK896799PARACERVICAL/PUDENDAL TRAYSK896559INFANT FEEDING TUBEK896794SPECIMEN CONTAINERK896806CATHETER PLUG/PROTECTORK896798TRACHEOSTOMY TRAY

View all 28 devices →

Related Devices (Code: LXG)

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.

K021927PLATELET CONCENTRATE SEPARATION KIT FOR CELSEP CENTRIFUGE SYSTEMBiomet, Inc.K943466MINI S.F.T. (URINE PRESERVATIVE)Cambridge Diagnostic Products, 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.

↑