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)

HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY

K-Number: K051103 · 2005-06-07

ApplicantHaag-Streit USA, Inc.
Decision Date2005-06-07
Product CodeHJK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Haag-Streit USA, Inc.. It received FDA 510(k) clearance on 2005-06-07 under 510(k) number K051103. The device is classified under product code HJK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY?

HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY is a medical device that received FDA 510(k) clearance on 2005-06-07. The listed applicant is Haag-Streit USA, Inc.. The 510(k) number is K051103.

When did HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY receive FDA 510(k) clearance?

HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY received FDA 510(k) clearance on 2005-06-07, under 510(k) number K051103.

Who is the listed applicant for HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY?

The FDA 510(k) record lists Haag-Streit USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY?

The FDA product code for HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY is HJK.

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

Related Devices (Code: HJK)

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.

K201909RxSight Contact LensRxsight, Inc.K173944Endocular Viewing Lenses and Silicone RingPhakosK051630SUPER VIEW DISPOSABLE BIOM LENS SETInsight Instruments, Inc.K050623VOLK DISPOSABLE VITRECTOMY LENSES, MODELS VOLK FLAT SSV D, VOLK AFX SSV D, VOLK 45 PRISM SSV DVolk Optical, Inc.K033950DORC VITRECTOMY LENSES, MODEL 1284 SERIESDutch Ophthalmic Research Center (D.O.R.C.)K030054DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSESFci Ophthalmics, Inc.

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.

↑