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FDA 510(k)

VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET

K-Number: K861745 · 1986-05-13

ApplicantKeeler Instruments, Inc.
Decision Date1986-05-13
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET 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 1986-05-13 under 510(k) number K861745. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET?

VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET is a medical device that received FDA 510(k) clearance on 1986-05-13. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K861745.

When did VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET receive FDA 510(k) clearance?

VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET received FDA 510(k) clearance on 1986-05-13, under 510(k) number K861745.

Who is the listed applicant for VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET?

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 VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET?

The FDA product code for VICKERS ERGOMATIC MICROSURG INSTRU CARDIAC SET is DWS.

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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: DWS)

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.

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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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