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)

SORBOTHANE VISCO INNER SOLE PAD

K-Number: K831552 · 1983-06-08

ApplicantFred Sammons, Inc.
Decision Date1983-06-08
Product CodeKNP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SORBOTHANE VISCO INNER SOLE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K831552. The device is classified under product code KNP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORBOTHANE VISCO INNER SOLE PAD?

SORBOTHANE VISCO INNER SOLE PAD is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K831552.

When did SORBOTHANE VISCO INNER SOLE PAD receive FDA 510(k) clearance?

SORBOTHANE VISCO INNER SOLE PAD received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831552.

Who is the listed applicant for SORBOTHANE VISCO INNER SOLE PAD?

The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORBOTHANE VISCO INNER SOLE PAD?

The FDA product code for SORBOTHANE VISCO INNER SOLE PAD is KNP.

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 Fred Sammons, Inc. 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.

K880644ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)K880647ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)K831549ARM SLINGSK831548SPLINTSK831550FINGER BONIOMETER BK7506K831544DELUXE TRACTION EXERCISE GLOVE BK5035

View all 278 devices →

Related Devices (Code: KNP)

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.

K831690IPOS ANTI-ADDUCTUS SHOEIpos LuneburgK823654SLIP-ON SANDALS FOR MEASURING SHORTNESSFred Sammons, Inc.K823665ROTATION BOOTWarm & Form, Orthopedic MaterialsK810228SORBOTHANEHamilton KentK801743PLASTAZOTE SHOEAlimed, Inc.K790326DRUSHOEJ.E. Hanger & Co. , Ltd.

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.

↑