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FDA 510(k)

3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW

K-Number: K871432 · 1987-08-07

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1987-08-07
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1987-08-07 under 510(k) number K871432. 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 3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW?

3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW is a medical device that received FDA 510(k) clearance on 1987-08-07. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K871432.

When did 3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW receive FDA 510(k) clearance?

3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW received FDA 510(k) clearance on 1987-08-07, under 510(k) number K871432.

Who is the listed applicant for 3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW?

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

What is the FDA product code for 3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW?

The FDA product code for 3.0 MHZ PHASED ARRAY SCANHEAD W/2.0 MHZ SIDEARM CW is ITX.

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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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