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FDA 510(k)

PODODIGITAL

K-Number: K864569 · 1987-02-04

ApplicantBroadwest Corp.
Decision Date1987-02-04
Product CodeIKE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PODODIGITAL is the device name listed in this FDA 510(k) record. The listed applicant is Broadwest Corp.. It received FDA 510(k) clearance on 1987-02-04 under 510(k) number K864569. The device is classified under product code IKE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PODODIGITAL?

PODODIGITAL is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Broadwest Corp.. The 510(k) number is K864569.

When did PODODIGITAL receive FDA 510(k) clearance?

PODODIGITAL received FDA 510(k) clearance on 1987-02-04, under 510(k) number K864569.

Who is the listed applicant for PODODIGITAL?

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

What is the FDA product code for PODODIGITAL?

The FDA product code for PODODIGITAL is IKE.

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 Broadwest Corp. 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.

K864499PODOSCOPEK852302INOX IORCEPS JARK852301INOX THERMOMETER JARK852300INOX IV STANDK851307INOX DRY HEAT STERILIZER

Related Devices (Code: IKE)

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.

K060125SONIC PALPOMETERPalpometer Systems, Inc.K954670PRESSORE MONITORCleveland Medical Devices, Inc.K915369THE EQUALIZERAdvanced Rehabilitative Technology, Inc.K915326PORTABLE LIMB LOAD MONITOR (BMLLM-100)Bar Med Pty , Ltd.K920091IOWA ORAL PERFORMANCE ISNTRUMENTBreakthrough, Inc.K915897FPLWrm Computers

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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