Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HYDRADJUST II UROLOGICAL TABLE

K-Number: K791699 · 1979-10-22

ApplicantSybron Corp.
Decision Date1979-10-22
Product CodeKQS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HYDRADJUST II UROLOGICAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1979-10-22 under 510(k) number K791699. 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 HYDRADJUST II UROLOGICAL TABLE?

HYDRADJUST II UROLOGICAL TABLE is a medical device that received FDA 510(k) clearance on 1979-10-22. The listed applicant is Sybron Corp.. The 510(k) number is K791699.

When did HYDRADJUST II UROLOGICAL TABLE receive FDA 510(k) clearance?

HYDRADJUST II UROLOGICAL TABLE received FDA 510(k) clearance on 1979-10-22, under 510(k) number K791699.

Who is the listed applicant for HYDRADJUST II UROLOGICAL TABLE?

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

What is the FDA product code for HYDRADJUST II UROLOGICAL TABLE?

The FDA product code for HYDRADJUST II UROLOGICAL TABLE is KQS.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sybron 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.

K862284SEALITEK854855PROOF ALGINATE IMPRESSION MATERIALK844092DIAGNOSTIC MICROSOPCE SLIDESK842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOK841910KERR SEALAPEX ROOT CANAL SEALERK841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

View all 37 devices →

Related Devices (Code: KQS)

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.

K955019UROTRACT IDornier Medtech America, Inc.K872022UROVIEWOec-Diasonics, Inc.K864846RADIOGRAPHIC - LEG SECTIONAmerican Sterilizer Co.K860040HYDRAJUST III UROLOGICAL TABLEMallinckrodt Group, Inc.K852127AMSCO URO-ENDO MOBILE TABLEAmerican Sterilizer Co.K801723UR 150-UR 150TSiemens Corp.

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.

↑