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FDA 510(k)

INFRAMETRICS INFRACAM-MED

K-Number: K982327 · 1998-08-18

Decision Date1998-08-18
Product CodeLHQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INFRAMETRICS INFRACAM-MED is the device name listed in this FDA 510(k) record. The listed applicant is Inframetrics, Inc.. It received FDA 510(k) clearance on 1998-08-18 under 510(k) number K982327. The device is classified under product code LHQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFRAMETRICS INFRACAM-MED?

INFRAMETRICS INFRACAM-MED is a medical device that received FDA 510(k) clearance on 1998-08-18. The listed applicant is Inframetrics, Inc.. The 510(k) number is K982327.

When did INFRAMETRICS INFRACAM-MED receive FDA 510(k) clearance?

INFRAMETRICS INFRACAM-MED received FDA 510(k) clearance on 1998-08-18, under 510(k) number K982327.

Who is the listed applicant for INFRAMETRICS INFRACAM-MED?

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

What is the FDA product code for INFRAMETRICS INFRACAM-MED?

The FDA product code for INFRAMETRICS INFRACAM-MED is LHQ.

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.

Related Devices (Code: LHQ)

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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