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FDA 510(k)

DUAL-TROL

K-Number: K802972 · 1981-01-15

ApplicantCimarron Instruments, Inc.
Decision Date1981-01-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DUAL-TROL is the device name listed in this FDA 510(k) record. The listed applicant is Cimarron Instruments, Inc.. It received FDA 510(k) clearance on 1981-01-15 under 510(k) number K802972. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL-TROL?

DUAL-TROL is a medical device that received FDA 510(k) clearance on 1981-01-15. The listed applicant is Cimarron Instruments, Inc.. The 510(k) number is K802972.

When did DUAL-TROL receive FDA 510(k) clearance?

DUAL-TROL received FDA 510(k) clearance on 1981-01-15, under 510(k) number K802972.

Who is the listed applicant for DUAL-TROL?

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

What is the FDA product code for DUAL-TROL?

The FDA product code for DUAL-TROL is GEI.

Other records listing Cimarron Instruments, 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.

K840545PAO BIPOLAR COAGULATORK801151DISPOSABLE SKIN RETRACTORK790293CIMARRON 1000 OR 1000-2

Related Devices (Code: GEI)

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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