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FDA 510(k)

MED-TEC HAND GRIP

K-Number: K954225 · 1995-11-14

ApplicantMedtec, Inc.
Decision Date1995-11-14
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MED-TEC HAND GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1995-11-14 under 510(k) number K954225. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-TEC HAND GRIP?

MED-TEC HAND GRIP is a medical device that received FDA 510(k) clearance on 1995-11-14. The listed applicant is Medtec, Inc.. The 510(k) number is K954225.

When did MED-TEC HAND GRIP receive FDA 510(k) clearance?

MED-TEC HAND GRIP received FDA 510(k) clearance on 1995-11-14, under 510(k) number K954225.

Who is the listed applicant for MED-TEC HAND GRIP?

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

What is the FDA product code for MED-TEC HAND GRIP?

The FDA product code for MED-TEC HAND GRIP is IXQ.

Other records listing Medtec, Inc. as applicant

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Related Devices (Code: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, Inc.K913425DIAL-A-RAD PORTA RAD TABLEDial-A-Rad

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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