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FDA 510(k)

RUBY KNIVES FOR OPHTH. SURGERY

K-Number: K832844 · 1983-09-29

ApplicantKeeler Instruments, Inc.
Decision Date1983-09-29
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RUBY KNIVES FOR OPHTH. SURGERY 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 1983-09-29 under 510(k) number K832844. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUBY KNIVES FOR OPHTH. SURGERY?

RUBY KNIVES FOR OPHTH. SURGERY is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K832844.

When did RUBY KNIVES FOR OPHTH. SURGERY receive FDA 510(k) clearance?

RUBY KNIVES FOR OPHTH. SURGERY received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832844.

Who is the listed applicant for RUBY KNIVES FOR OPHTH. SURGERY?

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 RUBY KNIVES FOR OPHTH. SURGERY?

The FDA product code for RUBY KNIVES FOR OPHTH. SURGERY is HNN.

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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: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, Inc.

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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