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FDA 510(k)

EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)

K-Number: K926218 · 1994-08-26

ApplicantSandhill Scientific, Inc.
Decision Date1994-08-26
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE) is the device name listed in this FDA 510(k) record. The listed applicant is Sandhill Scientific, Inc.. It received FDA 510(k) clearance on 1994-08-26 under 510(k) number K926218. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)?

EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE) is a medical device that received FDA 510(k) clearance on 1994-08-26. The listed applicant is Sandhill Scientific, Inc.. The 510(k) number is K926218.

When did EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE) receive FDA 510(k) clearance?

EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE) received FDA 510(k) clearance on 1994-08-26, under 510(k) number K926218.

Who is the listed applicant for EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)?

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

What is the FDA product code for EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)?

The FDA product code for EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE) is HIR.

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Other records listing Sandhill Scientific, Inc. as applicant

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Related Devices (Code: HIR)

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.

K252748Pelvic Floor Exerciser (PF01)Hunan Accurate Bio-Medical Technology Co., Ltd.K240805Flyte Mechanotherapy System, MTI-1.5 (MTI-1.5)Pelvital USA, Inc.K231875Vaginal Tactile Ultrasound ImagerAdvanced Tactile Imaging, Inc.K233362Flyte Mechanotherapy System (aka Flyte System) (MTI-1.0)Pelvital USA, Inc.K231780Perifit Care+X6 InnovationsK221476PerifitX6 Innovations

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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