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FDA 510(k)

3D1 MICROPOSITIONING HEADSTAGE

K-Number: K993501 · 1999-11-22

ApplicantScientific Tools, Inc.
Decision Date1999-11-22
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

3D1 MICROPOSITIONING HEADSTAGE is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Tools, Inc.. It received FDA 510(k) clearance on 1999-11-22 under 510(k) number K993501. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3D1 MICROPOSITIONING HEADSTAGE?

3D1 MICROPOSITIONING HEADSTAGE is a medical device that received FDA 510(k) clearance on 1999-11-22. The listed applicant is Scientific Tools, Inc.. The 510(k) number is K993501.

When did 3D1 MICROPOSITIONING HEADSTAGE receive FDA 510(k) clearance?

3D1 MICROPOSITIONING HEADSTAGE received FDA 510(k) clearance on 1999-11-22, under 510(k) number K993501.

Who is the listed applicant for 3D1 MICROPOSITIONING HEADSTAGE?

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

What is the FDA product code for 3D1 MICROPOSITIONING HEADSTAGE?

The FDA product code for 3D1 MICROPOSITIONING HEADSTAGE is HAW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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