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FDA 510(k)

HALL VEIN STRIPPER

K-Number: K872157 · 1987-07-07

ApplicantSolco Basle, Inc.
Decision Date1987-07-07
Product CodeDWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HALL VEIN STRIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Solco Basle, Inc.. It received FDA 510(k) clearance on 1987-07-07 under 510(k) number K872157. The device is classified under product code DWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL VEIN STRIPPER?

HALL VEIN STRIPPER is a medical device that received FDA 510(k) clearance on 1987-07-07. The listed applicant is Solco Basle, Inc.. The 510(k) number is K872157.

When did HALL VEIN STRIPPER receive FDA 510(k) clearance?

HALL VEIN STRIPPER received FDA 510(k) clearance on 1987-07-07, under 510(k) number K872157.

Who is the listed applicant for HALL VEIN STRIPPER?

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

What is the FDA product code for HALL VEIN STRIPPER?

The FDA product code for HALL VEIN STRIPPER is DWQ.

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Other records listing Solco Basle, Inc. as applicant

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Related Devices (Code: DWQ)

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.

K212894PhasTIPPLeMaitre Vascular, Inc.K041453SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023Smith & Nephew, Inc.K032387TRIVEX SYSTEMSmith & Nephew, Inc.K905528URESIL VALVE CUTTERUresil Corp.K904507PILLING BRUSH VALVULOTOMEPilling Co.K885046INSITUCAT VALVE STRIPPERAesculap Instruments Corp.

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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