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FDA 510(k)

RYDER LACRIMAL INTUBATIONSET

K-Number: K962151 · 1996-09-18

ApplicantRyder Intl. Corp.
Decision Date1996-09-18
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

RYDER LACRIMAL INTUBATIONSET is the device name listed in this FDA 510(k) record. The listed applicant is Ryder Intl. Corp.. It received FDA 510(k) clearance on 1996-09-18 under 510(k) number K962151. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RYDER LACRIMAL INTUBATIONSET?

RYDER LACRIMAL INTUBATIONSET is a medical device that received FDA 510(k) clearance on 1996-09-18. The listed applicant is Ryder Intl. Corp.. The 510(k) number is K962151.

When did RYDER LACRIMAL INTUBATIONSET receive FDA 510(k) clearance?

RYDER LACRIMAL INTUBATIONSET received FDA 510(k) clearance on 1996-09-18, under 510(k) number K962151.

Who is the listed applicant for RYDER LACRIMAL INTUBATIONSET?

The FDA 510(k) record lists Ryder Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RYDER LACRIMAL INTUBATIONSET?

The FDA product code for RYDER LACRIMAL INTUBATIONSET is OKS.

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Other records listing Ryder Intl. Corp. 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.

K962611BARD EAGLE INFLATION DEVICEK953522USCI IDEAL PTCA KITK920064OPTI-LENS CONTACT LENS CASEK915082OPTI-LENS(TM) CONTACT LENS CASEK881981ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEMK870278CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695

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Related Devices (Code: OKS)

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.

K201892Ritleng®+ and Ritleng®+ PVPFci (France Chirurgie Instrumentation) SasK201606LacriJet®Fci (France Chirurgie Instrumentation) SasK170247Lacriflow CLKaneka Pharma America, LLCK161373NunchakuFci (France Chirurgie Instrumentation)K160710Oasis Lacrimal Intubation SetAnodyneK130375SELF-RETAINING BICANALICULUS INTUBATON SET IIFci Sas (France Chirurgie Instrumentation)

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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