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FDA 510(k)

MICROPHOR

K-Number: K913601 · 1994-07-15

ApplicantLife-Tech Intl., Inc.
Decision Date1994-07-15
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROPHOR is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1994-07-15 under 510(k) number K913601. 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 MICROPHOR?

MICROPHOR is a medical device that received FDA 510(k) clearance on 1994-07-15. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K913601.

When did MICROPHOR receive FDA 510(k) clearance?

MICROPHOR received FDA 510(k) clearance on 1994-07-15, under 510(k) number K913601.

Who is the listed applicant for MICROPHOR?

The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROPHOR?

The FDA product code for MICROPHOR is EGJ.

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Other records listing Life-Tech Intl., 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.

K001129PROLONG, MODELS PL50, PL100, PL150K954505EZ STIMK955031MAXISTIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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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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