FDA 510(k)

RADIOGRAPHIC - LEG SECTION

K-Number: K864846 · 1986-12-24

Decision Date1986-12-24

Product CodeKQS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

RADIOGRAPHIC - LEG SECTION is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1986-12-24 under 510(k) number K864846. The device is classified under product code KQS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOGRAPHIC - LEG SECTION?

RADIOGRAPHIC - LEG SECTION is a medical device that received FDA 510(k) clearance on 1986-12-24. The listed applicant is American Sterilizer Co.. The 510(k) number is K864846.

When did RADIOGRAPHIC - LEG SECTION receive FDA 510(k) clearance?

RADIOGRAPHIC - LEG SECTION received FDA 510(k) clearance on 1986-12-24, under 510(k) number K864846.

Who is the listed applicant for RADIOGRAPHIC - LEG SECTION?

The FDA 510(k) record lists American Sterilizer Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RADIOGRAPHIC - LEG SECTION?

The FDA product code for RADIOGRAPHIC - LEG SECTION is KQS.

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Other records listing American Sterilizer Co. as applicant

K943288AMSCO SQ240 SURGICAL LIGHT K931872THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER K922485CHEMDI-VHP CHEMICAL INDICATOR K930493QUANTUM 3080 SURGICAL TABLE K905816ORTHOVISION TABLE K896674AMSCO QUANTUM LIGHT

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Related Devices (Code: KQS)

K955019UROTRACT IDornier Medtech America, Inc.K872022UROVIEWOec-Diasonics, Inc.K860040HYDRAJUST III UROLOGICAL TABLEMallinckrodt Group, Inc.K852127AMSCO URO-ENDO MOBILE TABLEAmerican Sterilizer Co.K801723UR 150-UR 150TSiemens Corp.K791699HYDRADJUST II UROLOGICAL TABLESybron Corp.

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.