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FDA 510(k)

ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.

K-Number: K900994 · 1990-08-15

ApplicantDlp, Inc.
Decision Date1990-08-15
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT. is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1990-08-15 under 510(k) number K900994. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.?

ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT. is a medical device that received FDA 510(k) clearance on 1990-08-15. The listed applicant is Dlp, Inc.. The 510(k) number is K900994.

When did ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT. receive FDA 510(k) clearance?

ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT. received FDA 510(k) clearance on 1990-08-15, under 510(k) number K900994.

Who is the listed applicant for ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.?

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

What is the FDA product code for ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.?

The FDA product code for ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT. is DTL.

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Other records listing Dlp, Inc. as applicant

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Related Devices (Code: DTL)

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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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