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FDA 510(k)

PHORESOR II (TM), MODEL PM700

K-Number: K872040 · 1987-08-04

ApplicantMotion Control, Inc.
Decision Date1987-08-04
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PHORESOR II (TM), MODEL PM700 is the device name listed in this FDA 510(k) record. The listed applicant is Motion Control, Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K872040. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHORESOR II (TM), MODEL PM700?

PHORESOR II (TM), MODEL PM700 is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Motion Control, Inc.. The 510(k) number is K872040.

When did PHORESOR II (TM), MODEL PM700 receive FDA 510(k) clearance?

PHORESOR II (TM), MODEL PM700 received FDA 510(k) clearance on 1987-08-04, under 510(k) number K872040.

Who is the listed applicant for PHORESOR II (TM), MODEL PM700?

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

What is the FDA product code for PHORESOR II (TM), MODEL PM700?

The FDA product code for PHORESOR II (TM), MODEL PM700 is EGJ.

Related Clinical Trials

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Other records listing Motion Control, 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.

K862236MYOLAB II, MODEL ML-200K802642UTAH ARTIFICAL ARMK780310DERMATRON IONTOPHORESIS DEVICE

Related Devices (Code: EGJ)

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.

K242041STOPWET iontophoresis apparatus (SW01)Taiwan Medical Electronics Co., Ltd.K241267Hidroxa SE30Hidroxa Medical ABK232020Iontophoresis ElectrodesTop-Rank Health Care Co., Ltd.K192749DermadryDermadry Laboratories, Inc.K191436SaalioSaalmann Medical GmbH & Co. KGK170835Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITEHightech Development

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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