FDA 510(k)

KNEE CUFF FOR EXPRESSING FLUID

K-Number: K770501 · 1977-04-05

Decision Date1977-04-05

Product Code

DecisionSubstantially Equivalent

Device Summary

KNEE CUFF FOR EXPRESSING FLUID is the device name listed in this FDA 510(k) record. The listed applicant is Robert R. Moore. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770501. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNEE CUFF FOR EXPRESSING FLUID?

KNEE CUFF FOR EXPRESSING FLUID is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Robert R. Moore. The 510(k) number is K770501.

When did KNEE CUFF FOR EXPRESSING FLUID receive FDA 510(k) clearance?

KNEE CUFF FOR EXPRESSING FLUID received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770501.

Who is the listed applicant for KNEE CUFF FOR EXPRESSING FLUID?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Robert R. Moore as applicant

K770658EXERCISER, LEG, LOWER EXTREMITY K770223HEAVY FOAM HEEL & ELBOW PROTECTORS K770060X-RAY POSITIONING DEVICE K770059ORTHOPEDIC SPECIALTIES

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.