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FDA 510(k)

BIOPSY NEEDLE TRANSPONDER SYSTEM

K-Number: K902214 · 1990-11-08

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1990-11-08
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BIOPSY NEEDLE TRANSPONDER SYSTEM 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 1990-11-08 under 510(k) number K902214. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY NEEDLE TRANSPONDER SYSTEM?

BIOPSY NEEDLE TRANSPONDER SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-08. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K902214.

When did BIOPSY NEEDLE TRANSPONDER SYSTEM receive FDA 510(k) clearance?

BIOPSY NEEDLE TRANSPONDER SYSTEM received FDA 510(k) clearance on 1990-11-08, under 510(k) number K902214.

Who is the listed applicant for BIOPSY NEEDLE TRANSPONDER SYSTEM?

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 BIOPSY NEEDLE TRANSPONDER SYSTEM?

The FDA product code for BIOPSY NEEDLE TRANSPONDER SYSTEM is IYO.

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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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