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FDA 510(k)

GERONIMO PR

K-Number: K935751 · 1995-02-03

ApplicantRedman, Inc.
Decision Date1995-02-03
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

GERONIMO PR is the device name listed in this FDA 510(k) record. The listed applicant is Redman, Inc.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K935751. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the GERONIMO PR?

GERONIMO PR is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Redman, Inc.. The 510(k) number is K935751.

When did GERONIMO PR receive FDA 510(k) clearance?

GERONIMO PR received FDA 510(k) clearance on 1995-02-03, under 510(k) number K935751.

Who is the listed applicant for GERONIMO PR?

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

What is the FDA product code for GERONIMO PR?

The FDA product code for GERONIMO PR is ITI.

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Other records listing Redman, Inc. as applicant

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Related Devices (Code: ITI)

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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