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FDA 510(k)

DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599

K-Number: K913447 · 1992-02-07

Decision Date1992-02-07
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599 is the device name listed in this FDA 510(k) record. The listed applicant is Graham Medical Products. It received FDA 510(k) clearance on 1992-02-07 under 510(k) number K913447. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599?

DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599 is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Graham Medical Products. The 510(k) number is K913447.

When did DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599 receive FDA 510(k) clearance?

DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599 received FDA 510(k) clearance on 1992-02-07, under 510(k) number K913447.

Who is the listed applicant for DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599?

The FDA 510(k) record lists Graham Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599?

The FDA product code for DISPOSABLE CYSTOSCOPY SPLASH DRAPE-STERILE #599 is KKX.

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 Graham Medical Products 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.

View all 9 devices →

Related Devices (Code: KKX)

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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