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)

THE TUCKER-SACH FOOT AND TUCKER-SYME FT

K-Number: K791331 · 1979-08-03

ApplicantKiswood Manufacturing, Inc.
Decision Date1979-08-03
Product CodeISH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE TUCKER-SACH FOOT AND TUCKER-SYME FT is the device name listed in this FDA 510(k) record. The listed applicant is Kiswood Manufacturing, Inc.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791331. The device is classified under product code ISH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TUCKER-SACH FOOT AND TUCKER-SYME FT?

THE TUCKER-SACH FOOT AND TUCKER-SYME FT is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Kiswood Manufacturing, Inc.. The 510(k) number is K791331.

When did THE TUCKER-SACH FOOT AND TUCKER-SYME FT receive FDA 510(k) clearance?

THE TUCKER-SACH FOOT AND TUCKER-SYME FT received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791331.

Who is the listed applicant for THE TUCKER-SACH FOOT AND TUCKER-SYME FT?

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

What is the FDA product code for THE TUCKER-SACH FOOT AND TUCKER-SYME FT?

The FDA product code for THE TUCKER-SACH FOOT AND TUCKER-SYME FT is ISH.

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

Related Devices (Code: ISH)

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.

K051256SILVERSEAL ORTHOTIC COMPONENT WITH X-STATICNoble Fiber Technologies, Inc.K823396FREE FLEX HEEL HEIGHT ADJUSTOROrthopedic Systems, Inc.K820505ANKLE/FOOT EXTERNALMauch Laboratories, 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.

↑