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)

AMT THERAPEUTIC TABLE, MODEL 748AMT

K-Number: K001401 · 2000-07-12

ApplicantAmt Mfg., Inc.
Decision Date2000-07-12
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AMT THERAPEUTIC TABLE, MODEL 748AMT is the device name listed in this FDA 510(k) record. The listed applicant is Amt Mfg., Inc.. It received FDA 510(k) clearance on 2000-07-12 under 510(k) number K001401. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMT THERAPEUTIC TABLE, MODEL 748AMT?

AMT THERAPEUTIC TABLE, MODEL 748AMT is a medical device that received FDA 510(k) clearance on 2000-07-12. The listed applicant is Amt Mfg., Inc.. The 510(k) number is K001401.

When did AMT THERAPEUTIC TABLE, MODEL 748AMT receive FDA 510(k) clearance?

AMT THERAPEUTIC TABLE, MODEL 748AMT received FDA 510(k) clearance on 2000-07-12, under 510(k) number K001401.

Who is the listed applicant for AMT THERAPEUTIC TABLE, MODEL 748AMT?

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

What is the FDA product code for AMT THERAPEUTIC TABLE, MODEL 748AMT?

The FDA product code for AMT THERAPEUTIC TABLE, MODEL 748AMT is ITH.

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: ITH)

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.

K243775True Non-Surgical Spinal Decompression System (DRX9000-SL)Excite Medical of Tampa Bay, LLCK243366DRX9000C-SL Cervical Spinal Decompression SystemExcite Medical of Tampa Bay, LLCK214037Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-TracErgo-Flex Technologies, LLCK222912c1TracZimmer Medizinsysteme GmbHK112074EVERYWAY TRACTION UNIT, MODEL EVER-TRAC ET-800Everyway Medical Instruments Co.,LtdK103248INTEGRITY SPINAL CARE SYSTEMIntegra Life Sciences

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.

↑