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FDA 510(k)

ELECTROSTIM 380

K-Number: K843488 · 1984-09-19

ApplicantMicron Instruments, Inc.
Decision Date1984-09-19
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTROSTIM 380 is the device name listed in this FDA 510(k) record. The listed applicant is Micron Instruments, Inc.. It received FDA 510(k) clearance on 1984-09-19 under 510(k) number K843488. 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 ELECTROSTIM 380?

ELECTROSTIM 380 is a medical device that received FDA 510(k) clearance on 1984-09-19. The listed applicant is Micron Instruments, Inc.. The 510(k) number is K843488.

When did ELECTROSTIM 380 receive FDA 510(k) clearance?

ELECTROSTIM 380 received FDA 510(k) clearance on 1984-09-19, under 510(k) number K843488.

Who is the listed applicant for ELECTROSTIM 380?

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

What is the FDA product code for ELECTROSTIM 380?

The FDA product code for ELECTROSTIM 380 is IPF.

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Other records listing Micron Instruments, 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.

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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

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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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