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FDA 510(k)

STIM-EX 201

K-Number: K800486 · 1980-03-19

ApplicantTh Charters, Inc.
Decision Date1980-03-19
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIM-EX 201 is the device name listed in this FDA 510(k) record. The listed applicant is Th Charters, Inc.. It received FDA 510(k) clearance on 1980-03-19 under 510(k) number K800486. 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 STIM-EX 201?

STIM-EX 201 is a medical device that received FDA 510(k) clearance on 1980-03-19. The listed applicant is Th Charters, Inc.. The 510(k) number is K800486.

When did STIM-EX 201 receive FDA 510(k) clearance?

STIM-EX 201 received FDA 510(k) clearance on 1980-03-19, under 510(k) number K800486.

Who is the listed applicant for STIM-EX 201?

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

What is the FDA product code for STIM-EX 201?

The FDA product code for STIM-EX 201 is IPF.

Other records listing Th Charters, Inc. as applicant

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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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