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FDA 510(k)

CALIBRE-TENTATIVE TRADENAME

K-Number: K833225 · 1984-02-28

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1984-02-28
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CALIBRE-TENTATIVE TRADENAME 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 1984-02-28 under 510(k) number K833225. 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 CALIBRE-TENTATIVE TRADENAME?

CALIBRE-TENTATIVE TRADENAME is a medical device that received FDA 510(k) clearance on 1984-02-28. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K833225.

When did CALIBRE-TENTATIVE TRADENAME receive FDA 510(k) clearance?

CALIBRE-TENTATIVE TRADENAME received FDA 510(k) clearance on 1984-02-28, under 510(k) number K833225.

Who is the listed applicant for CALIBRE-TENTATIVE TRADENAME?

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 CALIBRE-TENTATIVE TRADENAME?

The FDA product code for CALIBRE-TENTATIVE TRADENAME 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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