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FDA 510(k)

THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER)

K-Number: K863989 · 1986-10-31

ApplicantKeeler Instruments, Inc.
Decision Date1986-10-31
Product CodeHNC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER) is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K863989. The device is classified under product code HNC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER)?

THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER) is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K863989.

When did THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER) receive FDA 510(k) clearance?

THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER) received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863989.

Who is the listed applicant for THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER)?

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

What is the FDA product code for THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER)?

The FDA product code for THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER) is HNC.

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Other records listing Keeler Instruments, 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.

K181143Keeler TonoCare TonometerK112093CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTERK093298PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000K100500PSL CLASSIC SLIT LAMPK062412CRYOMATICK060822VANTAGE INDIRECT OPHTHALMOSCOPE

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Related Devices (Code: HNC)

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.

K022836STEPHENS DISPOSABLE SPECULUMStephens InstrumentsK981235OCULOSTATLaser Center Dev. Corp.K964289EYE FIXATION SPECULUMEyefix, Inc.K863664OPHTHALMIC SURGICAL SPECULUMMyocure, Inc.K843196VISITEC EYE SPECULUMVisitec Co.K830430EYELID SPECULUMDouglas C. Mckee & 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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