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FDA 510(k)

DAVID SIMMONDS ANESTHESIA EXTENSION TUBES

K-Number: K905384 · 1991-03-22

ApplicantSparta Surgical Corp.
Decision Date1991-03-22
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DAVID SIMMONDS ANESTHESIA EXTENSION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Sparta Surgical Corp.. It received FDA 510(k) clearance on 1991-03-22 under 510(k) number K905384. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVID SIMMONDS ANESTHESIA EXTENSION TUBES?

DAVID SIMMONDS ANESTHESIA EXTENSION TUBES is a medical device that received FDA 510(k) clearance on 1991-03-22. The listed applicant is Sparta Surgical Corp.. The 510(k) number is K905384.

When did DAVID SIMMONDS ANESTHESIA EXTENSION TUBES receive FDA 510(k) clearance?

DAVID SIMMONDS ANESTHESIA EXTENSION TUBES received FDA 510(k) clearance on 1991-03-22, under 510(k) number K905384.

Who is the listed applicant for DAVID SIMMONDS ANESTHESIA EXTENSION TUBES?

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

What is the FDA product code for DAVID SIMMONDS ANESTHESIA EXTENSION TUBES?

The FDA product code for DAVID SIMMONDS ANESTHESIA EXTENSION TUBES is FMF.

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Other records listing Sparta Surgical Corp. 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.

K965187SPECTRUM II, SPECTRUM PLUS, AND SPECTRUM MAX-SDK945313SPARTA HYDROGEL WOUND DRESSINGK922729SPARTA WET DRESSING, SODIUM CHLORIDEK905240VESSELOOPSK896085SURGI-BRUSHK896084MICROSPEARS

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Related Devices (Code: FMF)

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.

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLCK252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.

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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