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FDA 510(k)

THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE

K-Number: K932149 · 1995-05-11

ApplicantThought Technology , Ltd.
Decision Date1995-05-11
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Thought Technology , Ltd.. It received FDA 510(k) clearance on 1995-05-11 under 510(k) number K932149. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE?

THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1995-05-11. The listed applicant is Thought Technology , Ltd.. The 510(k) number is K932149.

When did THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE receive FDA 510(k) clearance?

THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE received FDA 510(k) clearance on 1995-05-11, under 510(k) number K932149.

Who is the listed applicant for THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE?

The FDA 510(k) record lists Thought Technology , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE?

The FDA product code for THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE is HIR.

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Related Devices (Code: HIR)

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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