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FDA 510(k)

BURTON AUTOMATIC PROJECTOR - MODEL CP-40

K-Number: K924774 · 1993-04-14

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

Device Summary

BURTON AUTOMATIC PROJECTOR - MODEL CP-40 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 K924774. The device is classified under product code HOD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURTON AUTOMATIC PROJECTOR - MODEL CP-40?

BURTON AUTOMATIC PROJECTOR - MODEL CP-40 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 K924774.

When did BURTON AUTOMATIC PROJECTOR - MODEL CP-40 receive FDA 510(k) clearance?

BURTON AUTOMATIC PROJECTOR - MODEL CP-40 received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924774.

Who is the listed applicant for BURTON AUTOMATIC PROJECTOR - MODEL CP-40?

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 AUTOMATIC PROJECTOR - MODEL CP-40?

The FDA product code for BURTON AUTOMATIC PROJECTOR - MODEL CP-40 is HOD.

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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 1990K924783BURTON SLIT LAMP - MODEL 850K924786BURTON TRIAL LENS SETK924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000K924784BURTON PROJECTOR HEAD - MODEL 6000-HK924778BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8

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Related Devices (Code: HOD)

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.

K891610HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENERKeeler Instruments, Inc.K831285SURGICAL/LID MARGIN COVER & EYELASH-Richard R. Anthony, M.D.

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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