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FDA 510(k)

STRIPE PROJECTOR

K-Number: K902138 · 1990-07-05

ApplicantAcademic Catalyst Corp.
Decision Date1990-07-05
Product CodeHJI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STRIPE PROJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Academic Catalyst Corp.. It received FDA 510(k) clearance on 1990-07-05 under 510(k) number K902138. The device is classified under product code HJI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRIPE PROJECTOR?

STRIPE PROJECTOR is a medical device that received FDA 510(k) clearance on 1990-07-05. The listed applicant is Academic Catalyst Corp.. The 510(k) number is K902138.

When did STRIPE PROJECTOR receive FDA 510(k) clearance?

STRIPE PROJECTOR received FDA 510(k) clearance on 1990-07-05, under 510(k) number K902138.

Who is the listed applicant for STRIPE PROJECTOR?

The FDA 510(k) record lists Academic Catalyst Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRIPE PROJECTOR?

The FDA product code for STRIPE PROJECTOR is HJI.

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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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