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FDA 510(k)

HOFFMAN IVF-1

K-Number: K991216 · 1999-08-05

Applicant(Arms) Hoffman Surgical Equipment, Ivf Division
Decision Date1999-08-05
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HOFFMAN IVF-1 is the device name listed in this FDA 510(k) record. The listed applicant is (Arms) Hoffman Surgical Equipment, Ivf Division. It received FDA 510(k) clearance on 1999-08-05 under 510(k) number K991216. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOFFMAN IVF-1?

HOFFMAN IVF-1 is a medical device that received FDA 510(k) clearance on 1999-08-05. The listed applicant is (Arms) Hoffman Surgical Equipment, Ivf Division. The 510(k) number is K991216.

When did HOFFMAN IVF-1 receive FDA 510(k) clearance?

HOFFMAN IVF-1 received FDA 510(k) clearance on 1999-08-05, under 510(k) number K991216.

Who is the listed applicant for HOFFMAN IVF-1?

The FDA 510(k) record lists (Arms) Hoffman Surgical Equipment, Ivf Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOFFMAN IVF-1?

The FDA product code for HOFFMAN IVF-1 is MQG.

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Related Devices (Code: MQG)

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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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