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FDA 510(k)

ANNULAR ARRAY SCANHEAD

K-Number: K871856 · 1987-08-28

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1987-08-28
Product CodeHGL
Advisory CommitteeOB
DecisionSubstantially Equivalent for Some Indications

Device Summary

ANNULAR ARRAY SCANHEAD 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 1987-08-28 under 510(k) number K871856. The device is classified under product code HGL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ANNULAR ARRAY SCANHEAD?

ANNULAR ARRAY SCANHEAD is a medical device that received FDA 510(k) clearance on 1987-08-28. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K871856.

When did ANNULAR ARRAY SCANHEAD receive FDA 510(k) clearance?

ANNULAR ARRAY SCANHEAD received FDA 510(k) clearance on 1987-08-28, under 510(k) number K871856.

Who is the listed applicant for ANNULAR ARRAY SCANHEAD?

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 ANNULAR ARRAY SCANHEAD?

The FDA product code for ANNULAR ARRAY SCANHEAD is HGL.

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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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