Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VISTA UNIVERSAL HANDPIECE

K-Number: K972252 · 1997-07-29

ApplicantOdyssey Technologies, Inc.
Decision Date1997-07-29
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISTA UNIVERSAL HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Odyssey Technologies, Inc.. It received FDA 510(k) clearance on 1997-07-29 under 510(k) number K972252. 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 VISTA UNIVERSAL HANDPIECE?

VISTA UNIVERSAL HANDPIECE is a medical device that received FDA 510(k) clearance on 1997-07-29. The listed applicant is Odyssey Technologies, Inc.. The 510(k) number is K972252.

When did VISTA UNIVERSAL HANDPIECE receive FDA 510(k) clearance?

VISTA UNIVERSAL HANDPIECE received FDA 510(k) clearance on 1997-07-29, under 510(k) number K972252.

Who is the listed applicant for VISTA UNIVERSAL HANDPIECE?

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

What is the FDA product code for VISTA UNIVERSAL HANDPIECE?

The FDA product code for VISTA UNIVERSAL HANDPIECE is HQC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Odyssey Technologies, Inc. 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.

K972253P3 UNIVERSAL PHACO HANDPIECE

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.

↑