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FDA 510(k)

MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300

K-Number: K893491 · 1989-06-22

ApplicantCuda Products Co.
Decision Date1989-06-22
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300 is the device name listed in this FDA 510(k) record. The listed applicant is Cuda Products Co.. It received FDA 510(k) clearance on 1989-06-22 under 510(k) number K893491. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300?

MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300 is a medical device that received FDA 510(k) clearance on 1989-06-22. The listed applicant is Cuda Products Co.. The 510(k) number is K893491.

When did MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300 receive FDA 510(k) clearance?

MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300 received FDA 510(k) clearance on 1989-06-22, under 510(k) number K893491.

Who is the listed applicant for MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300?

The FDA 510(k) record lists Cuda Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300?

The FDA product code for MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300 is FST.

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Other records listing Cuda Products Co. as applicant

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Related Devices (Code: FST)

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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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