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FDA 510(k)

VAX-T PELVIC TRACTION BELT

K-Number: K894435 · 1989-08-03

ApplicantVat-Tech, Inc.
Decision Date1989-08-03
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VAX-T PELVIC TRACTION BELT is the device name listed in this FDA 510(k) record. The listed applicant is Vat-Tech, Inc.. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K894435. 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 VAX-T PELVIC TRACTION BELT?

VAX-T PELVIC TRACTION BELT is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Vat-Tech, Inc.. The 510(k) number is K894435.

When did VAX-T PELVIC TRACTION BELT receive FDA 510(k) clearance?

VAX-T PELVIC TRACTION BELT received FDA 510(k) clearance on 1989-08-03, under 510(k) number K894435.

Who is the listed applicant for VAX-T PELVIC TRACTION BELT?

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

What is the FDA product code for VAX-T PELVIC TRACTION BELT?

The FDA product code for VAX-T PELVIC TRACTION BELT 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.

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Other records listing Vat-Tech, 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.

K951622VAX-D THERAPEUTIC TABLE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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