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FDA 510(k)

LAPAROSCOPIC CATHERTER

K-Number: K903187 · 1990-10-12

ApplicantCook Ob/Gyn
Decision Date1990-10-12
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC CATHERTER is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K903187. 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 LAPAROSCOPIC CATHERTER?

LAPAROSCOPIC CATHERTER is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Cook Ob/Gyn. The 510(k) number is K903187.

When did LAPAROSCOPIC CATHERTER receive FDA 510(k) clearance?

LAPAROSCOPIC CATHERTER received FDA 510(k) clearance on 1990-10-12, under 510(k) number K903187.

Who is the listed applicant for LAPAROSCOPIC CATHERTER?

The FDA 510(k) record lists Cook Ob/Gyn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC CATHERTER?

The FDA product code for LAPAROSCOPIC CATHERTER is 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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