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FDA 510(k)

PERCUTANEOUS CATHETER INSERTION TRAY

K-Number: K831729 · 1983-07-18

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1983-07-18
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS CATHETER INSERTION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K831729. 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 CATHETER INSERTION TRAY?

PERCUTANEOUS CATHETER INSERTION TRAY is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K831729.

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

PERCUTANEOUS CATHETER INSERTION TRAY received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831729.

Who is the listed applicant for PERCUTANEOUS CATHETER INSERTION TRAY?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERCUTANEOUS CATHETER INSERTION TRAY?

The FDA product code for PERCUTANEOUS CATHETER INSERTION TRAY is DQY.

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Other records listing American Pharmaseal Div. Ahsc as applicant

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Related Devices (Code: DQY)

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.

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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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