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FDA 510(k)

LASER LAPAROSCOPY SET

K-Number: K873598 · 1988-01-20

ApplicantCuda Products Co.
Decision Date1988-01-20
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LASER LAPAROSCOPY SET 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 1988-01-20 under 510(k) number K873598. 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 LASER LAPAROSCOPY SET?

LASER LAPAROSCOPY SET is a medical device that received FDA 510(k) clearance on 1988-01-20. The listed applicant is Cuda Products Co.. The 510(k) number is K873598.

When did LASER LAPAROSCOPY SET receive FDA 510(k) clearance?

LASER LAPAROSCOPY SET received FDA 510(k) clearance on 1988-01-20, under 510(k) number K873598.

Who is the listed applicant for LASER LAPAROSCOPY SET?

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 LASER LAPAROSCOPY SET?

The FDA product code for LASER LAPAROSCOPY SET is HET.

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Other records listing Cuda Products Co. as applicant

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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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