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FDA 510(k)

CABOT FIBER LASER PROBE

K-Number: K873115 · 1988-01-28

ApplicantCabot Medical Corp.
Decision Date1988-01-28
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CABOT FIBER LASER PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1988-01-28 under 510(k) number K873115. 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 CABOT FIBER LASER PROBE?

CABOT FIBER LASER PROBE is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Cabot Medical Corp.. The 510(k) number is K873115.

When did CABOT FIBER LASER PROBE receive FDA 510(k) clearance?

CABOT FIBER LASER PROBE received FDA 510(k) clearance on 1988-01-28, under 510(k) number K873115.

Who is the listed applicant for CABOT FIBER LASER PROBE?

The FDA 510(k) record lists Cabot Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CABOT FIBER LASER PROBE?

The FDA product code for CABOT FIBER LASER PROBE is HET.

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Other records listing Cabot Medical Corp. 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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