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FDA 510(k)

BURTON TRIAL LENS SET

K-Number: K924786 · 1993-04-14

ApplicantR.H. Burton Co.
Decision Date1993-04-14
Product CodeHPC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BURTON TRIAL LENS SET is the device name listed in this FDA 510(k) record. The listed applicant is R.H. Burton Co.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K924786. The device is classified under product code HPC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURTON TRIAL LENS SET?

BURTON TRIAL LENS SET is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is R.H. Burton Co.. The 510(k) number is K924786.

When did BURTON TRIAL LENS SET receive FDA 510(k) clearance?

BURTON TRIAL LENS SET received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924786.

Who is the listed applicant for BURTON TRIAL LENS SET?

The FDA 510(k) record lists R.H. Burton Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BURTON TRIAL LENS SET?

The FDA product code for BURTON TRIAL LENS SET is HPC.

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Other records listing R.H. Burton Co. 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.

K924773BURTON H- BASE TABLE - MODEL 1990K924774BURTON AUTOMATIC PROJECTOR - MODEL CP-40K924783BURTON SLIT LAMP - MODEL 850K924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000K924784BURTON PROJECTOR HEAD - MODEL 6000-HK924778BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8

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Related Devices (Code: HPC)

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.

K945443BOBES LENS SETBobes S.A.K951437OTI MODEL TLS-60Oti Medical, LLCK930195OPHTHALMIC TRIAL LENSESOptimark Accessories and InstrumentsK934859CONTACT LENSESArno Intl., Inc.K930446MARCO TRIAL SETSMarco Ophthalmic, Inc.K920571TRIAL LENS SETR.H. Burton Co.

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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