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FDA 510(k)

REVERSING CLICK GENERATOR RCG6

K-Number: K771188 · 1977-07-14

ApplicantTeca, Inc.
Decision Date1977-07-14
Product CodeETS
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

REVERSING CLICK GENERATOR RCG6 is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771188. The device is classified under product code ETS. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVERSING CLICK GENERATOR RCG6?

REVERSING CLICK GENERATOR RCG6 is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Teca, Inc.. The 510(k) number is K771188.

When did REVERSING CLICK GENERATOR RCG6 receive FDA 510(k) clearance?

REVERSING CLICK GENERATOR RCG6 received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771188.

Who is the listed applicant for REVERSING CLICK GENERATOR RCG6?

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

What is the FDA product code for REVERSING CLICK GENERATOR RCG6?

The FDA product code for REVERSING CLICK GENERATOR RCG6 is ETS.

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Other records listing Teca, 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: ETS)

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.

K813557AUDITORY STIMULATORWestern Advanced Technology, Inc.K811790OCTOTOXIC SCREENERWestern Advanced Technology, Inc.K811772AUDITORY LOCALIZERWestern Advanced Technology, Inc.K790064TINNITUS DEVICESVicon Instrument Co.

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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