FDA 510(k)

CO2 LAPAROSCOPE

K-Number: K841668 · 1984-04-23

Decision Date1984-04-23

Product Code

DecisionUnknown

Device Summary

CO2 LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Laser Spectrum, Inc.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K841668. FDA Decision: Unknown.

Frequently Asked Questions

What is the CO2 LAPAROSCOPE?

CO2 LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Laser Spectrum, Inc.. The 510(k) number is K841668.

When did CO2 LAPAROSCOPE receive FDA 510(k) clearance?

CO2 LAPAROSCOPE received FDA 510(k) clearance on 1984-04-23, under 510(k) number K841668.

Who is the listed applicant for CO2 LAPAROSCOPE?

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

Related Clinical Trials

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Other records listing Laser Spectrum, Inc. as applicant

K863520CO2 LASER MICROMANIPULATOR K844765ACCESSORY SET FOR CO2 LASER BRONCHOSCOPY INSTRUMEN K841781MODEL 305AA PORTABLE LASER K842498DANIELL DBL PUNCTURE LASER LAPAROSCOPY

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.