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FDA 510(k)

TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG

K-Number: K852680 · 1985-12-23

ApplicantMultigon Industries, Inc.
Decision Date1985-12-23
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG is the device name listed in this FDA 510(k) record. The listed applicant is Multigon Industries, Inc.. It received FDA 510(k) clearance on 1985-12-23 under 510(k) number K852680. 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 TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG?

TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG is a medical device that received FDA 510(k) clearance on 1985-12-23. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K852680.

When did TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG receive FDA 510(k) clearance?

TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG received FDA 510(k) clearance on 1985-12-23, under 510(k) number K852680.

Who is the listed applicant for TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG?

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

What is the FDA product code for TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG?

The FDA product code for TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG is HET.

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Other records listing Multigon Industries, 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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