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FDA 510(k)

CARR RIGID CONTAINER SYSTEM

K-Number: K972138 · 1997-11-13

ApplicantCarr Metal Products, Inc.
Decision Date1997-11-13
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CARR RIGID CONTAINER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Carr Metal Products, Inc.. It received FDA 510(k) clearance on 1997-11-13 under 510(k) number K972138. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARR RIGID CONTAINER SYSTEM?

CARR RIGID CONTAINER SYSTEM is a medical device that received FDA 510(k) clearance on 1997-11-13. The listed applicant is Carr Metal Products, Inc.. The 510(k) number is K972138.

When did CARR RIGID CONTAINER SYSTEM receive FDA 510(k) clearance?

CARR RIGID CONTAINER SYSTEM received FDA 510(k) clearance on 1997-11-13, under 510(k) number K972138.

Who is the listed applicant for CARR RIGID CONTAINER SYSTEM?

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

What is the FDA product code for CARR RIGID CONTAINER SYSTEM?

The FDA product code for CARR RIGID CONTAINER SYSTEM is FRG.

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.

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Other records listing Carr Metal Products, Inc. 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.

K023658STERILIZATION CASES AND TRAYS

Related Devices (Code: FRG)

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

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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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