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FDA 510(k)

MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR

K-Number: K912044 · 1991-06-24

Decision Date1991-06-24
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR 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 1991-06-24 under 510(k) number K912044. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR?

MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR is a medical device that received FDA 510(k) clearance on 1991-06-24. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K912044.

When did MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR receive FDA 510(k) clearance?

MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR received FDA 510(k) clearance on 1991-06-24, under 510(k) number K912044.

Who is the listed applicant for MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR?

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 MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR?

The FDA product code for MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR is HIF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Multigon Industries, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: HIF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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