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FDA 510(k)

RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE

K-Number: K925505 · 1993-09-02

ApplicantRusch, Inc.
Decision Date1993-09-02
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE is the device name listed in this FDA 510(k) record. The listed applicant is Rusch, Inc.. It received FDA 510(k) clearance on 1993-09-02 under 510(k) number K925505. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE?

RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE is a medical device that received FDA 510(k) clearance on 1993-09-02. The listed applicant is Rusch, Inc.. The 510(k) number is K925505.

When did RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE receive FDA 510(k) clearance?

RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE received FDA 510(k) clearance on 1993-09-02, under 510(k) number K925505.

Who is the listed applicant for RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE?

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

What is the FDA product code for RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE?

The FDA product code for RUSCH SAFETY CLEAR PLUS CUFFED W/MURPHY EYE is BTR.

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.

Other records listing Rusch, 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.

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Related Devices (Code: BTR)

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.

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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