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FDA 510(k)

USCI IDEAL PTCA KIT

K-Number: K953522 · 1996-04-17

ApplicantRyder Intl. Corp.
Decision Date1996-04-17
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI IDEAL PTCA KIT 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 1996-04-17 under 510(k) number K953522. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USCI IDEAL PTCA KIT?

USCI IDEAL PTCA KIT is a medical device that received FDA 510(k) clearance on 1996-04-17. The listed applicant is Ryder Intl. Corp.. The 510(k) number is K953522.

When did USCI IDEAL PTCA KIT receive FDA 510(k) clearance?

USCI IDEAL PTCA KIT received FDA 510(k) clearance on 1996-04-17, under 510(k) number K953522.

Who is the listed applicant for USCI IDEAL PTCA KIT?

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 USCI IDEAL PTCA KIT?

The FDA product code for USCI IDEAL PTCA KIT is MAV.

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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 DEVICEK962151RYDER LACRIMAL INTUBATIONSETK920064OPTI-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: MAV)

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.

K260035Digital Indeflator INFLANTEUAB TelemedicinaK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)Medtronic VascularK162272Fluent inflation deviceVascular Solutions, Inc.K153038Everest 20 Disposable Inflation Device, Everest 20 Survival Kit, Everest 30 Disposable Inflation Device, Everest 30 Survival KitMedtronic, Inc.K153672basixTOUCH40 Inflation SyringeMerit Medical Systems, Inc.K130566BASIXTOUCHMerit Medical Systems, 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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