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FDA 510(k)

PERCUTANEOUS INTRODUCER TRAY

K-Number: K904608 · 1990-12-03

ApplicantThomas Medical Products, Inc.
Decision Date1990-12-03
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS INTRODUCER TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Thomas Medical Products, Inc.. It received FDA 510(k) clearance on 1990-12-03 under 510(k) number K904608. 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 PERCUTANEOUS INTRODUCER TRAY?

PERCUTANEOUS INTRODUCER TRAY is a medical device that received FDA 510(k) clearance on 1990-12-03. The listed applicant is Thomas Medical Products, Inc.. The 510(k) number is K904608.

When did PERCUTANEOUS INTRODUCER TRAY receive FDA 510(k) clearance?

PERCUTANEOUS INTRODUCER TRAY received FDA 510(k) clearance on 1990-12-03, under 510(k) number K904608.

Who is the listed applicant for PERCUTANEOUS INTRODUCER TRAY?

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

What is the FDA product code for PERCUTANEOUS INTRODUCER TRAY?

The FDA product code for PERCUTANEOUS INTRODUCER TRAY is DQY.

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Other records listing Thomas Medical Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K122431HEARTSPAN STEERABLE INTRODUCER KITK120158CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITSK101015GUIDE CATHETERS AND ACCESSORIESK083269CROSSOVERK081341REINFORCED CATHETER INTRODUCER SYSTEM (RCIS)K072745Y-GLIDE

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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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