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FDA 510(k)

GRIESHABER GLOBAL CONTROL TUBING SET

K-Number: K863444 · 1986-10-31

ApplicantGrieshaber & Co.
Decision Date1986-10-31
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GRIESHABER GLOBAL CONTROL TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K863444. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER GLOBAL CONTROL TUBING SET?

GRIESHABER GLOBAL CONTROL TUBING SET is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Grieshaber & Co.. The 510(k) number is K863444.

When did GRIESHABER GLOBAL CONTROL TUBING SET receive FDA 510(k) clearance?

GRIESHABER GLOBAL CONTROL TUBING SET received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863444.

Who is the listed applicant for GRIESHABER GLOBAL CONTROL TUBING SET?

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

What is the FDA product code for GRIESHABER GLOBAL CONTROL TUBING SET?

The FDA product code for GRIESHABER GLOBAL CONTROL TUBING SET is HQC.

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Other records listing Grieshaber & Co. 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.

K950056THE GRIESHABER AXIAL CUTTERK930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEK914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEK914587GRIESHABER AIR/FLUID TUBING SETK914586GRIESHABER THREE FUNCTION MANIPULATORK914585GRIESHABER TWO FUNCTION MANIPULATOR

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Related Devices (Code: HQC)

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.

K261264Stellaris Elite™ vision enhancement system; Posterior and Combined Procedure Pack(s): 23 ga. Posterior Elite™ Pack (SE5423); 23 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423B); 25 ga. Posterior Elite™ Pack (SE5425); 25 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5425B); 27 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5427B); 23 ga. Bi-Blade™+ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423BB+); 25 ga. Bi-Blade™+Bausch and LombK252052Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)Bausch and Lomb, IncorporatedK250501System SophiThis AGK243395MICOR 700 with Auto I/ACarl Zeiss Meditec Cataract Technology, Inc.K242801MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)Carl Zeiss Meditec Cataract Technology, Inc.K240169Stellaris Elite vision enhancement system (BL11145, BL14455, BL15455)Bausch and Lomb, Incorporated

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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