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FDA 510(k)

RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)

K-Number: K951560 · 1995-04-17

ApplicantRadius Intl., Inc.
Decision Date1995-04-17
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) is the device name listed in this FDA 510(k) record. The listed applicant is Radius Intl., Inc.. It received FDA 510(k) clearance on 1995-04-17 under 510(k) number K951560. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)?

RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) is a medical device that received FDA 510(k) clearance on 1995-04-17. The listed applicant is Radius Intl., Inc.. The 510(k) number is K951560.

When did RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) receive FDA 510(k) clearance?

RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) received FDA 510(k) clearance on 1995-04-17, under 510(k) number K951560.

Who is the listed applicant for RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)?

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

What is the FDA product code for RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)?

The FDA product code for RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) is IOR.

Related Clinical Trials

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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Other records listing Radius Intl., 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.

K972102RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK972025RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK971901RADIUS LOW PROFILE GASTROSTOMY TUBE KITK930510RADIUS ENTERAL FEEDING TUBE

Related Devices (Code: IOR)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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