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FDA 510(k)

BAHO AUTOCLAVABLE LAPAROSCOPE

K-Number: K982276 · 1999-02-18

ApplicantMicroptix Int'L, LLC
Decision Date1999-02-18
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BAHO AUTOCLAVABLE LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Microptix Int'L, LLC. It received FDA 510(k) clearance on 1999-02-18 under 510(k) number K982276. 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 BAHO AUTOCLAVABLE LAPAROSCOPE?

BAHO AUTOCLAVABLE LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1999-02-18. The listed applicant is Microptix Int'L, LLC. The 510(k) number is K982276.

When did BAHO AUTOCLAVABLE LAPAROSCOPE receive FDA 510(k) clearance?

BAHO AUTOCLAVABLE LAPAROSCOPE received FDA 510(k) clearance on 1999-02-18, under 510(k) number K982276.

Who is the listed applicant for BAHO AUTOCLAVABLE LAPAROSCOPE?

The FDA 510(k) record lists Microptix Int'L, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAHO AUTOCLAVABLE LAPAROSCOPE?

The FDA product code for BAHO AUTOCLAVABLE LAPAROSCOPE is HET.

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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.

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