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FDA 510(k)

PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP

K-Number: K992174 · 2000-03-23

ApplicantPilling Weck Surgical
Decision Date2000-03-23
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP 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 2000-03-23 under 510(k) number K992174. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP?

PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP is a medical device that received FDA 510(k) clearance on 2000-03-23. The listed applicant is Pilling Weck Surgical. The 510(k) number is K992174.

When did PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP receive FDA 510(k) clearance?

PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP received FDA 510(k) clearance on 2000-03-23, under 510(k) number K992174.

Who is the listed applicant for PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP?

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 AORTIC SPOON-JAW CLAMP?

The FDA product code for PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP is DXC.

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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.

K992476PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADSK990935JACKSON ESOPHAGEAL DILATORK990561OPTICAL FORCEPSK982128SHIKANI-FRENCH SPEAKING VALVE

Related Devices (Code: DXC)

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.

K262086PreludeSYNC™ Radial Compression DeviceMerit Medical Systems, Inc.K260105Fogarty Spring Clips, Handleless Clamps, and Clamp InsertsEdwards LifesciencesK252772Arc Adjustable Radial Cuff Compression DeviceTz Medical, Inc.K254060Life Saving TourniquetTW MedicalK243627Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)Arc Trauma, LLCK253070Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)Medline Industries, LP

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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