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FDA 510(k)

FOOT VALVE

K-Number: K790195 · 1979-02-26

ApplicantAmerican Safety
Decision Date1979-02-26
Product CodeGET
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FOOT VALVE is the device name listed in this FDA 510(k) record. The listed applicant is American Safety. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K790195. The device is classified under product code GET. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOOT VALVE?

FOOT VALVE is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is American Safety. The 510(k) number is K790195.

When did FOOT VALVE receive FDA 510(k) clearance?

FOOT VALVE received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790195.

Who is the listed applicant for FOOT VALVE?

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

What is the FDA product code for FOOT VALVE?

The FDA product code for FOOT VALVE is GET.

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 American Safety 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.

K760210BLANKET, WATER-JEL FIRE

Related Devices (Code: GET)

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.

K960473AESCULAP POWER SYSTEM HANDPIECEAesculap, Inc.K955174SODEM HIGH SPEED SYSTEM FOR NEUROSURGERY & MEDIAN STYERNOTOMYSodem Diffusion SAK942987NUCLEOTOME L KITSurgical Dynamics, Inc.K954076MIDAS REX DRILL ATTACHMENTS & TWIST DRILLSMidas Rex Pneumatic Tools, Inc.K953433MIDAS REX TELESCOPING SYSTEMMidas Rex Pneumatic Tools, Inc.K953432ROTATING, FIXED FOOTED, FIXED SHIELD ATTACHMENTS, DISSECTING TOOLSMidas Rex Pneumatic Tools, Inc.

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.

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