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FDA 510(k)

HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR

K-Number: K872441 · 1988-02-19

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1988-02-19
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR 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 1988-02-19 under 510(k) number K872441. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR?

HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR is a medical device that received FDA 510(k) clearance on 1988-02-19. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K872441.

When did HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR receive FDA 510(k) clearance?

HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR received FDA 510(k) clearance on 1988-02-19, under 510(k) number K872441.

Who is the listed applicant for HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR?

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 HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR?

The FDA product code for HIGH FREQ LINEAR ARRAY(HFLA)SCANHEAD W/DPLR SIDEAR is DPT.

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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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