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FDA 510(k)

SURGITEK ALL SILICONE INFECTION DOUBJ

K-Number: K833782 · 1984-04-02

ApplicantSurgitek
Decision Date1984-04-02
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGITEK ALL SILICONE INFECTION DOUBJ is the device name listed in this FDA 510(k) record. The listed applicant is Surgitek. It received FDA 510(k) clearance on 1984-04-02 under 510(k) number K833782. 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 SURGITEK ALL SILICONE INFECTION DOUBJ?

SURGITEK ALL SILICONE INFECTION DOUBJ is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Surgitek. The 510(k) number is K833782.

When did SURGITEK ALL SILICONE INFECTION DOUBJ receive FDA 510(k) clearance?

SURGITEK ALL SILICONE INFECTION DOUBJ received FDA 510(k) clearance on 1984-04-02, under 510(k) number K833782.

Who is the listed applicant for SURGITEK ALL SILICONE INFECTION DOUBJ?

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

What is the FDA product code for SURGITEK ALL SILICONE INFECTION DOUBJ?

The FDA product code for SURGITEK ALL SILICONE INFECTION DOUBJ is FAD.

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Other records listing Surgitek 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.

K946296QUADRA-COIL URETERAL STENTK944391OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEMK943491RIGHT ANGLE UROLOGIC LASER FIBERK941952SURGITEK INFUSERK933260HELICAL STONE/FLATWIRE STONE BASKETSK933261GRASPING FORCEPS

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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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