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FDA 510(k)

LARES AIR PRESSURE GAUGE

K-Number: K801534 · 1980-07-14

ApplicantLares Manufacturing Co., Inc.
Decision Date1980-07-14
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LARES AIR PRESSURE GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Lares Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1980-07-14 under 510(k) number K801534. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARES AIR PRESSURE GAUGE?

LARES AIR PRESSURE GAUGE is a medical device that received FDA 510(k) clearance on 1980-07-14. The listed applicant is Lares Manufacturing Co., Inc.. The 510(k) number is K801534.

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

LARES AIR PRESSURE GAUGE received FDA 510(k) clearance on 1980-07-14, under 510(k) number K801534.

Who is the listed applicant for LARES AIR PRESSURE GAUGE?

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

What is the FDA product code for LARES AIR PRESSURE GAUGE?

The FDA product code for LARES AIR PRESSURE GAUGE is EIA.

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Other records listing Lares Manufacturing Co., 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.

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Related Devices (Code: EIA)

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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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