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FDA 510(k)

SONIC PALPOMETER

K-Number: K060125 · 2006-03-16

ApplicantPalpometer Systems, Inc.
Decision Date2006-03-16
Product CodeIKE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SONIC PALPOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Palpometer Systems, Inc.. It received FDA 510(k) clearance on 2006-03-16 under 510(k) number K060125. 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 SONIC PALPOMETER?

SONIC PALPOMETER is a medical device that received FDA 510(k) clearance on 2006-03-16. The listed applicant is Palpometer Systems, Inc.. The 510(k) number is K060125.

When did SONIC PALPOMETER receive FDA 510(k) clearance?

SONIC PALPOMETER received FDA 510(k) clearance on 2006-03-16, under 510(k) number K060125.

Who is the listed applicant for SONIC PALPOMETER?

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

What is the FDA product code for SONIC PALPOMETER?

The FDA product code for SONIC PALPOMETER is IKE.

Related Clinical Trials

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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.

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 ComputersK914780TALLEY SD.500 SKIN PRESSURE EVALUATORTalley Group, Ltd.

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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