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FDA 510(k)

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO

K-Number: K881010 · 1988-04-21

ApplicantSharplan Lasers, Inc.
Decision Date1988-04-21
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO is the device name listed in this FDA 510(k) record. The listed applicant is Sharplan Lasers, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881010. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO?

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K881010.

When did CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO receive FDA 510(k) clearance?

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881010.

Who is the listed applicant for CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO?

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

What is the FDA product code for CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO?

The FDA product code for CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO is HET.

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Other records listing Sharplan Lasers, Inc. as applicant

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Related Devices (Code: HET)

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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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