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FDA 510(k)

PRESSURE GAUGE

K-Number: K921026 · 1992-04-24

ApplicantHobbs Medical, Inc.
Decision Date1992-04-24
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PRESSURE GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Hobbs Medical, Inc.. It received FDA 510(k) clearance on 1992-04-24 under 510(k) number K921026. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE GAUGE?

PRESSURE GAUGE is a medical device that received FDA 510(k) clearance on 1992-04-24. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K921026.

When did PRESSURE GAUGE receive FDA 510(k) clearance?

PRESSURE GAUGE received FDA 510(k) clearance on 1992-04-24, under 510(k) number K921026.

Who is the listed applicant for PRESSURE GAUGE?

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

What is the FDA product code for PRESSURE GAUGE?

The FDA product code for PRESSURE GAUGE is KNT.

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Related Devices (Code: KNT)

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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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