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FDA 510(k)

TITAN AIR SPECTACLE FRAME

K-Number: K896350 · 1989-12-18

ApplicantAcces Intl. Eyewear
Decision Date1989-12-18
Product CodeHQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TITAN AIR SPECTACLE FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Acces Intl. Eyewear. It received FDA 510(k) clearance on 1989-12-18 under 510(k) number K896350. The device is classified under product code HQJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITAN AIR SPECTACLE FRAME?

TITAN AIR SPECTACLE FRAME is a medical device that received FDA 510(k) clearance on 1989-12-18. The listed applicant is Acces Intl. Eyewear. The 510(k) number is K896350.

When did TITAN AIR SPECTACLE FRAME receive FDA 510(k) clearance?

TITAN AIR SPECTACLE FRAME received FDA 510(k) clearance on 1989-12-18, under 510(k) number K896350.

Who is the listed applicant for TITAN AIR SPECTACLE FRAME?

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

What is the FDA product code for TITAN AIR SPECTACLE FRAME?

The FDA product code for TITAN AIR SPECTACLE FRAME is HQJ.

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 Acces Intl. Eyewear 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.

K903173LAURENT TARDY

Related Devices (Code: HQJ)

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.

K884362LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLDBausch & Lomb Pharmaceutical, Inc.K875014LABTICIAN RETINAL IMPLANTSLabtician Products, Inc.K831773MAI HYDROSEAL IMPLANT FOR SCLERAL BUCKBcd Products, Inc.K760550IMPLANT, SILICONE AND TANTALUMMedical Instrument Research Assoc., 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.

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