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FDA 510(k)

INTRODUCER

K-Number: K951090 · 1995-07-11

ApplicantRanfac, Corp.
Decision Date1995-07-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac, Corp.. It received FDA 510(k) clearance on 1995-07-11 under 510(k) number K951090. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRODUCER?

INTRODUCER is a medical device that received FDA 510(k) clearance on 1995-07-11. The listed applicant is Ranfac, Corp.. The 510(k) number is K951090.

When did INTRODUCER receive FDA 510(k) clearance?

INTRODUCER received FDA 510(k) clearance on 1995-07-11, under 510(k) number K951090.

Who is the listed applicant for INTRODUCER?

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

What is the FDA product code for INTRODUCER?

The FDA product code for INTRODUCER is GCJ.

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Other records listing Ranfac, 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.

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Related Devices (Code: GCJ)

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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