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FDA 510(k)

TBD, LENS MEASURING DEVICE

K-Number: K912134 · 1991-07-25

ApplicantAlcon Laboratories
Decision Date1991-07-25
Product CodeHRJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TBD, LENS MEASURING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1991-07-25 under 510(k) number K912134. The device is classified under product code HRJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TBD, LENS MEASURING DEVICE?

TBD, LENS MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1991-07-25. The listed applicant is Alcon Laboratories. The 510(k) number is K912134.

When did TBD, LENS MEASURING DEVICE receive FDA 510(k) clearance?

TBD, LENS MEASURING DEVICE received FDA 510(k) clearance on 1991-07-25, under 510(k) number K912134.

Who is the listed applicant for TBD, LENS MEASURING DEVICE?

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

What is the FDA product code for TBD, LENS MEASURING DEVICE?

The FDA product code for TBD, LENS MEASURING DEVICE is HRJ.

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Other records listing Alcon Laboratories 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.

K062624NEXT GENERATION LASERK062865SMALL VOLUME SYRINGEK000148RGP MULTI-PURPOSE SOLUTION ID 100136K984573OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROPK990480OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVERK984575MULTI-PURPOSE DISINFECTING SOLUTION ID 90746

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Related Devices (Code: HRJ)

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.

K930447MARCO H AND TS-1 INSTRUMENT TABLESMarco Ophthalmic, Inc.K922242910T MONTORIZED INSTRUMENT TABLER.H. Burton Co.K853744TECHNA VISION, INC.ELECTRIC TABLETechna VisionK853359RELIANCE 1379Dentsply Intl.K841760WOODLYN CLASSIC INSTRUMENT STANDWoodlyn, Inc.K833820MACHEMER/TANO ROTATINGOptical Micro Systems, 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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