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FDA 510(k)

VERSASTAT MULTIPOLAR SCISSORS AND CABLES

K-Number: K974250 · 1998-02-11

ApplicantPilling Weck, Inc.
Decision Date1998-02-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VERSASTAT MULTIPOLAR SCISSORS AND CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Weck, Inc.. It received FDA 510(k) clearance on 1998-02-11 under 510(k) number K974250. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSASTAT MULTIPOLAR SCISSORS AND CABLES?

VERSASTAT MULTIPOLAR SCISSORS AND CABLES is a medical device that received FDA 510(k) clearance on 1998-02-11. The listed applicant is Pilling Weck, Inc.. The 510(k) number is K974250.

When did VERSASTAT MULTIPOLAR SCISSORS AND CABLES receive FDA 510(k) clearance?

VERSASTAT MULTIPOLAR SCISSORS AND CABLES received FDA 510(k) clearance on 1998-02-11, under 510(k) number K974250.

Who is the listed applicant for VERSASTAT MULTIPOLAR SCISSORS AND CABLES?

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

What is the FDA product code for VERSASTAT MULTIPOLAR SCISSORS AND CABLES?

The FDA product code for VERSASTAT MULTIPOLAR SCISSORS AND CABLES is GEI.

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Other records listing Pilling Weck, Inc. 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.

K990547PILLING WECK SURGICAL Y STENT FORCEPSK962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSK945520HEMOCLIP ECOSYSTEMK944552PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIPK943719VISISTAT STAPLER

Related Devices (Code: GEI)

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.

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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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