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FDA 510(k)

TRAY, DISPOSABLE

K-Number: K760498 · 1976-11-02

ApplicantArgon Medical Corp.
Decision Date1976-11-02
Product Code
DecisionSubstantially Equivalent

Device Summary

TRAY, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760498. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAY, DISPOSABLE?

TRAY, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is Argon Medical Corp.. The 510(k) number is K760498.

When did TRAY, DISPOSABLE receive FDA 510(k) clearance?

TRAY, DISPOSABLE received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760498.

Who is the listed applicant for TRAY, DISPOSABLE?

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

Related Clinical Trials

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Other records listing Argon Medical Corp. 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.

K904994CLOSED SYSTEM FLUSH SETK895511CATHETER BALLOON DILATOR PRESSURE GAUGEK894157OBTURATORK891022INTRODUCER FOR PTCA GUIDING CATHETERSK884375TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETERK882221OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE

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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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