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FDA 510(k)

SURGITEKS PERCUTANEOUS ANTEGRADE ALL -

K-Number: K830884 · 1983-05-09

ApplicantMedical Engineering Corp.
Decision Date1983-05-09
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGITEKS PERCUTANEOUS ANTEGRADE ALL - is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Corp.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K830884. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGITEKS PERCUTANEOUS ANTEGRADE ALL -?

SURGITEKS PERCUTANEOUS ANTEGRADE ALL - is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Medical Engineering Corp.. The 510(k) number is K830884.

When did SURGITEKS PERCUTANEOUS ANTEGRADE ALL - receive FDA 510(k) clearance?

SURGITEKS PERCUTANEOUS ANTEGRADE ALL - received FDA 510(k) clearance on 1983-05-09, under 510(k) number K830884.

Who is the listed applicant for SURGITEKS PERCUTANEOUS ANTEGRADE ALL -?

The FDA 510(k) record lists Medical Engineering Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGITEKS PERCUTANEOUS ANTEGRADE ALL -?

The FDA product code for SURGITEKS PERCUTANEOUS ANTEGRADE ALL - is FAD.

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Other records listing Medical Engineering Corp. as applicant

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K934141STAND ALONE CYSTOMETROGRAMK905289SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENTK903448SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDERK902773SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SETK884746SURGITEK FLAT T-SPANK883274SURGITEK (R) UROFLOW SYSTEM

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Related Devices (Code: FAD)

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.

K251890Disposable Ureteral StentsZhejiang Chuangxiang Medical Technology Co., Ltd.K251469Endura™ Ureteral Stent and Stent SetCathegenix (Xiamen) Co., Ltd.K243039Ureteral Stents (AF-D series)Alton (Shanghai) Medical Instruments Co., Ltd.K243830Disposable ureteral stentShenzhen Trious Medical Technology Co., Ltd.K250824Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDrive Steerable Ureteral Stent Set; Contour Ureteral Stent; Contour SureDrive Steerable Ureteral Stent Set; Contour VL Variable Length Ureteral Stent; Contour VL SureDrive Steerable Ureteral Stent Set; Polaris Ultra Ureteral Stent; Polaris Loop Ureteral Stent; Tria Firm Ureteral Stent; Tria Soft Ureteral Stent; Percuflex Urinary Diversion Stent SetBoston Scientific CorporationK232920RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmUreteral Stent Company

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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