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FDA 510(k)

NIIC CO2 LASER SYSTEM MODEL 3OZ.

K-Number: K827914 · 1982-09-13

ApplicantCooper Lasersonics, Inc.
Decision Date1982-09-13
Product Code
DecisionSubstantially Equivalent

Device Summary

NIIC CO2 LASER SYSTEM MODEL 3OZ. is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Lasersonics, Inc.. It received FDA 510(k) clearance on 1982-09-13 under 510(k) number K827914. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIIC CO2 LASER SYSTEM MODEL 3OZ.?

NIIC CO2 LASER SYSTEM MODEL 3OZ. is a medical device that received FDA 510(k) clearance on 1982-09-13. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K827914.

When did NIIC CO2 LASER SYSTEM MODEL 3OZ. receive FDA 510(k) clearance?

NIIC CO2 LASER SYSTEM MODEL 3OZ. received FDA 510(k) clearance on 1982-09-13, under 510(k) number K827914.

Who is the listed applicant for NIIC CO2 LASER SYSTEM MODEL 3OZ.?

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

Related Clinical Trials

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Other records listing Cooper Lasersonics, 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.

K880808ILLUMINA MODEL 40 CO2 LASER FOR GENERAL/PLASTIC SUK880427ILLUMINA 40 CO2 LASER SYSTEMK880428ILLUMINA 25 CO2 LASER SYSTEMK880429ILLUMINA 55 CO2 LASER SYSTEMK880807ILLUMINA MODEL 25 CO2 LASER FOR GENERAL/PLASTIC SUK880809ILLUMINA MODEL 55 CO2 LASER FOR GENERAL/PLASTIC SU

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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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