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FDA 510(k)

ESCOTEK-EST 204 MULTI STIM

K-Number: K844390 · 1985-05-07

ApplicantNor-Am Patient Care Products, Inc.
Decision Date1985-05-07
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ESCOTEK-EST 204 MULTI STIM is the device name listed in this FDA 510(k) record. The listed applicant is Nor-Am Patient Care Products, Inc.. It received FDA 510(k) clearance on 1985-05-07 under 510(k) number K844390. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESCOTEK-EST 204 MULTI STIM?

ESCOTEK-EST 204 MULTI STIM is a medical device that received FDA 510(k) clearance on 1985-05-07. The listed applicant is Nor-Am Patient Care Products, Inc.. The 510(k) number is K844390.

When did ESCOTEK-EST 204 MULTI STIM receive FDA 510(k) clearance?

ESCOTEK-EST 204 MULTI STIM received FDA 510(k) clearance on 1985-05-07, under 510(k) number K844390.

Who is the listed applicant for ESCOTEK-EST 204 MULTI STIM?

The FDA 510(k) record lists Nor-Am Patient Care Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESCOTEK-EST 204 MULTI STIM?

The FDA product code for ESCOTEK-EST 204 MULTI STIM is IPF.

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Other records listing Nor-Am Patient Care Products, 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.

K900647SOUTHERN CROSS HI-V4 PULSED HIGH VOLTAGE GALVANICK844389ESCOTEK EST 210, HIGH VOLTAGE ELECTRO GALVANIC STIK844388ESCOTEK EST 220 INTERFERENCE THERAPY UNITK844387ESCOTEK-EST 221 VACUUM UNITK844385ESCOTEK EST TRAC 401K844386ESCOTEK-EST 301A ULTRA-SONIC UNIT

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Related Devices (Code: IPF)

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.

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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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