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)

PROJECTOR, ACCU-CHART ACUITY

K-Number: K781658 · 1978-10-17

ApplicantBausch & Lomb, Inc.
Decision Date1978-10-17
Product CodeHOS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PROJECTOR, ACCU-CHART ACUITY is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1978-10-17 under 510(k) number K781658. The device is classified under product code HOS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROJECTOR, ACCU-CHART ACUITY?

PROJECTOR, ACCU-CHART ACUITY is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K781658.

When did PROJECTOR, ACCU-CHART ACUITY receive FDA 510(k) clearance?

PROJECTOR, ACCU-CHART ACUITY received FDA 510(k) clearance on 1978-10-17, under 510(k) number K781658.

Who is the listed applicant for PROJECTOR, ACCU-CHART ACUITY?

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

What is the FDA product code for PROJECTOR, ACCU-CHART ACUITY?

The FDA product code for PROJECTOR, ACCU-CHART ACUITY is HOS.

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 Bausch & Lomb, 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.

K192005Bausch + Lomb PreVue Inserter for enVista PreloadedK173480Crystalsert Lens Delivery SystemK161012Easy-Load Lens Delivery SystemK131208BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,K122575BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VIK113852BAUSCH & LOMB IOL INJECTOR

View all 92 devices →

Related Devices (Code: HOS)

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.

K936200WIRELESS CHART PROJECTOR,HCP-W 721Canon USA, Inc.K930443MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJEMarco Ophthalmic, Inc.K924784BURTON PROJECTOR HEAD - MODEL 6000-HR.H. Burton Co.K921214OPHTHALMIC PROJECTORLuneau Ophtalmologie SAK890992WOODLYN OPHTHALMIC PROJECTORWoodlyn, Inc.K862519BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTORBausch & Lomb, 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.

↑