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FDA 510(k)

JACE TRI-STIM DEVICE

K-Number: K931781 · 1993-10-08

ApplicantJace Systems, Inc.
Decision Date1993-10-08
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JACE TRI-STIM DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Jace Systems, Inc.. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K931781. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACE TRI-STIM DEVICE?

JACE TRI-STIM DEVICE is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Jace Systems, Inc.. The 510(k) number is K931781.

When did JACE TRI-STIM DEVICE receive FDA 510(k) clearance?

JACE TRI-STIM DEVICE received FDA 510(k) clearance on 1993-10-08, under 510(k) number K931781.

Who is the listed applicant for JACE TRI-STIM DEVICE?

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

What is the FDA product code for JACE TRI-STIM DEVICE?

The FDA product code for JACE TRI-STIM DEVICE is IPF.

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 Jace Systems, 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.

K933059ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD.K931016JACE MODEL H440 HAND CPM DEVICEK922185JACE KNEE EXTENSION SYSTEM -- MODIFICATIONK921351JACE MODEL PM-410 HAND CPM DEVICEK920380JACE MODEL W550 WRIST CPM DEVICE

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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