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FDA 510(k)

MINISTIM 180

K-Number: K822924 · 1982-12-13

ApplicantMicron Instruments, Inc.
Decision Date1982-12-13
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MINISTIM 180 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 1982-12-13 under 510(k) number K822924. 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 MINISTIM 180?

MINISTIM 180 is a medical device that received FDA 510(k) clearance on 1982-12-13. The listed applicant is Micron Instruments, Inc.. The 510(k) number is K822924.

When did MINISTIM 180 receive FDA 510(k) clearance?

MINISTIM 180 received FDA 510(k) clearance on 1982-12-13, under 510(k) number K822924.

Who is the listed applicant for MINISTIM 180?

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 MINISTIM 180?

The FDA product code for MINISTIM 180 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.

K843488ELECTROSTIM 380K810044MUSCLE STIMULATOR

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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