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FDA 510(k)

DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000

K-Number: K894131 · 1989-09-26

ApplicantThermedics, Inc.
Decision Date1989-09-26
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Thermedics, Inc.. It received FDA 510(k) clearance on 1989-09-26 under 510(k) number K894131. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000?

DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000 is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Thermedics, Inc.. The 510(k) number is K894131.

When did DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000 receive FDA 510(k) clearance?

DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000 received FDA 510(k) clearance on 1989-09-26, under 510(k) number K894131.

Who is the listed applicant for DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000?

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

What is the FDA product code for DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000?

The FDA product code for DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000 is DQY.

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Other records listing Thermedics, Inc. as applicant

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Related Devices (Code: DQY)

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Official Source

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