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FDA 510(k)

CIMARRON 1000 OR 1000-2

K-Number: K790293 · 1979-04-12

ApplicantCimarron Instruments, Inc.
Decision Date1979-04-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CIMARRON 1000 OR 1000-2 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 1979-04-12 under 510(k) number K790293. 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 CIMARRON 1000 OR 1000-2?

CIMARRON 1000 OR 1000-2 is a medical device that received FDA 510(k) clearance on 1979-04-12. The listed applicant is Cimarron Instruments, Inc.. The 510(k) number is K790293.

When did CIMARRON 1000 OR 1000-2 receive FDA 510(k) clearance?

CIMARRON 1000 OR 1000-2 received FDA 510(k) clearance on 1979-04-12, under 510(k) number K790293.

Who is the listed applicant for CIMARRON 1000 OR 1000-2?

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 CIMARRON 1000 OR 1000-2?

The FDA product code for CIMARRON 1000 OR 1000-2 is GEI.

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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 COAGULATORK802972DUAL-TROLK801151DISPOSABLE SKIN RETRACTOR

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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