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FDA 510(k)

VALTRAC(R) INTRODUCER FORCEP

K-Number: K922348 · 1992-06-09

Decision Date1992-06-09
Product CodeHJE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALTRAC(R) INTRODUCER FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is American Cyanamid Co.. It received FDA 510(k) clearance on 1992-06-09 under 510(k) number K922348. The device is classified under product code HJE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALTRAC(R) INTRODUCER FORCEP?

VALTRAC(R) INTRODUCER FORCEP is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is American Cyanamid Co.. The 510(k) number is K922348.

When did VALTRAC(R) INTRODUCER FORCEP receive FDA 510(k) clearance?

VALTRAC(R) INTRODUCER FORCEP received FDA 510(k) clearance on 1992-06-09, under 510(k) number K922348.

Who is the listed applicant for VALTRAC(R) INTRODUCER FORCEP?

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

What is the FDA product code for VALTRAC(R) INTRODUCER FORCEP?

The FDA product code for VALTRAC(R) INTRODUCER FORCEP is HJE.

Related Clinical Trials

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.

Other records listing American Cyanamid Co. 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.

View all 7 devices →

Related Devices (Code: HJE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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