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FDA 510(k)

TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS

K-Number: K014182 · 2002-01-03

ApplicantTetrad Corp.
Decision Date2002-01-03
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS is the device name listed in this FDA 510(k) record. The listed applicant is Tetrad Corp.. It received FDA 510(k) clearance on 2002-01-03 under 510(k) number K014182. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS?

TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS is a medical device that received FDA 510(k) clearance on 2002-01-03. The listed applicant is Tetrad Corp.. The 510(k) number is K014182.

When did TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS receive FDA 510(k) clearance?

TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS received FDA 510(k) clearance on 2002-01-03, under 510(k) number K014182.

Who is the listed applicant for TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS?

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

What is the FDA product code for TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS?

The FDA product code for TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS is ITX.

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Other records listing Tetrad Corp. 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.

K042620SONATA 3-D IMAGING ACCESSORY, MODEL 3DSK013849TETRAD MODEL TC-EC7-ACP, -L5-, -L7-, -V4-ACP TRANSDUCERSK002193TETRAD TC-C3-ACP

Related Devices (Code: ITX)

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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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