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FDA 510(k)

PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS

K-Number: K992476 · 2000-09-13

ApplicantPilling Weck Surgical
Decision Date2000-09-13
Product CodeMWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Weck Surgical. It received FDA 510(k) clearance on 2000-09-13 under 510(k) number K992476. The device is classified under product code MWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS?

PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS is a medical device that received FDA 510(k) clearance on 2000-09-13. The listed applicant is Pilling Weck Surgical. The 510(k) number is K992476.

When did PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS receive FDA 510(k) clearance?

PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS received FDA 510(k) clearance on 2000-09-13, under 510(k) number K992476.

Who is the listed applicant for PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS?

The FDA 510(k) record lists Pilling Weck Surgical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS?

The FDA product code for PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS is MWS.

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 Pilling Weck Surgical 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.

K992174PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMPK990935JACKSON ESOPHAGEAL DILATORK990561OPTICAL FORCEPSK982128SHIKANI-FRENCH SPEAKING VALVE

Related Devices (Code: MWS)

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.

K041338MEDTRONIC OCTOPUS TE STABILIZER & ACCESSORIESMedtronic VascularK992833VACUUM ASSIST STABILIZERCardio Thoracic SystemsK982419HEART-LIFT BALLOON POSITIONERCardiothoracic Systems, 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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