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)

PHYACTION 787

K-Number: K930670 · 1993-07-02

ApplicantVerimed Holdings, Inc.
Decision Date1993-07-02
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PHYACTION 787 is the device name listed in this FDA 510(k) record. The listed applicant is Verimed Holdings, Inc.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K930670. 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 PHYACTION 787?

PHYACTION 787 is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Verimed Holdings, Inc.. The 510(k) number is K930670.

When did PHYACTION 787 receive FDA 510(k) clearance?

PHYACTION 787 received FDA 510(k) clearance on 1993-07-02, under 510(k) number K930670.

Who is the listed applicant for PHYACTION 787?

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

What is the FDA product code for PHYACTION 787?

The FDA product code for PHYACTION 787 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.

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

Other records listing Verimed Holdings, 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.

K981277PERIFORMK954127BIOFEEDBACK DEVICEK951969MYOEXORCISER II FUALK922550ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)K913912VERIMED PERINEOMETERK893220VERIMED MYOEXORCISER VERISTIM

View all 12 devices →

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

View on FDA Database →

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

↑