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FDA 510(k)

AKRON ATP9 TRACTION MACHINE

K-Number: K992733 · 1999-11-10

ApplicantHuntleigh Technology, Inc.
Decision Date1999-11-10
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AKRON ATP9 TRACTION MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1999-11-10 under 510(k) number K992733. 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 AKRON ATP9 TRACTION MACHINE?

AKRON ATP9 TRACTION MACHINE is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K992733.

When did AKRON ATP9 TRACTION MACHINE receive FDA 510(k) clearance?

AKRON ATP9 TRACTION MACHINE received FDA 510(k) clearance on 1999-11-10, under 510(k) number K992733.

Who is the listed applicant for AKRON ATP9 TRACTION MACHINE?

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

What is the FDA product code for AKRON ATP9 TRACTION MACHINE?

The FDA product code for AKRON ATP9 TRACTION MACHINE is ITH.

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Other records listing Huntleigh Technology, 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.

K964699RHEO DOPPLEX II (RD 2)K924516OP3/VP4K910188FLOWPLUS AC330 PUMP GARMENTSK900882MULTI DOPPLEX, MD-1K900618HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140K890012HUNTLEIGH DYNAMIC FLOTATION SYSTEM

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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.

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