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FDA 510(k)

BURTON OPHTHALMIC EXAM UNIT - MODEL 2201

K-Number: K924780 · 1993-04-05

ApplicantR.H. Burton Co.
Decision Date1993-04-05
Product CodeHMF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BURTON OPHTHALMIC EXAM UNIT - MODEL 2201 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 1993-04-05 under 510(k) number K924780. The device is classified under product code HMF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURTON OPHTHALMIC EXAM UNIT - MODEL 2201?

BURTON OPHTHALMIC EXAM UNIT - MODEL 2201 is a medical device that received FDA 510(k) clearance on 1993-04-05. The listed applicant is R.H. Burton Co.. The 510(k) number is K924780.

When did BURTON OPHTHALMIC EXAM UNIT - MODEL 2201 receive FDA 510(k) clearance?

BURTON OPHTHALMIC EXAM UNIT - MODEL 2201 received FDA 510(k) clearance on 1993-04-05, under 510(k) number K924780.

Who is the listed applicant for BURTON OPHTHALMIC EXAM UNIT - MODEL 2201?

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 OPHTHALMIC EXAM UNIT - MODEL 2201?

The FDA product code for BURTON OPHTHALMIC EXAM UNIT - MODEL 2201 is HMF.

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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-40K924786BURTON TRIAL LENS SETK924783BURTON SLIT LAMP - MODEL 850K924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000K924784BURTON PROJECTOR HEAD - MODEL 6000-H

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Related Devices (Code: HMF)

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.

K935952ROTA SYSTEM 5000Rota Systems Medfurniture, Inc.K935945ROTA DATAMATE IRota Systems,Inc.K931839ROTA SYSTEM XLRota Systems Medfurniture, Inc.K930440MARCO INTERNATIONAL STANDMarco Ophthalmic, Inc.K924771BURTON OPHTHALMIC STAND - MODEL XL3200R.H. Burton Co.K913961OPHTHALMIC STANDLuneau Ophtalmologie SA

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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