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FDA 510(k)

RELIEF VALVE-HONAN INTRAOC. PRESSURE

K-Number: K820526 · 1982-03-25

ApplicantThe Lebanon Corp.
Decision Date1982-03-25
Product CodeLCC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RELIEF VALVE-HONAN INTRAOC. PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is The Lebanon Corp.. It received FDA 510(k) clearance on 1982-03-25 under 510(k) number K820526. The device is classified under product code LCC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIEF VALVE-HONAN INTRAOC. PRESSURE?

RELIEF VALVE-HONAN INTRAOC. PRESSURE is a medical device that received FDA 510(k) clearance on 1982-03-25. The listed applicant is The Lebanon Corp.. The 510(k) number is K820526.

When did RELIEF VALVE-HONAN INTRAOC. PRESSURE receive FDA 510(k) clearance?

RELIEF VALVE-HONAN INTRAOC. PRESSURE received FDA 510(k) clearance on 1982-03-25, under 510(k) number K820526.

Who is the listed applicant for RELIEF VALVE-HONAN INTRAOC. PRESSURE?

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

What is the FDA product code for RELIEF VALVE-HONAN INTRAOC. PRESSURE?

The FDA product code for RELIEF VALVE-HONAN INTRAOC. PRESSURE is LCC.

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.

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Other records listing The Lebanon Corp. 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.

K841652OCULAR PRESSURE APPLICATORK821689LEBANON MICROSCOPE

Related Devices (Code: LCC)

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.

K112952ILWAIT TIMER OCULOPRESSOROryx Medical Pty, Ltd.K946194WEE BAG O'MERCURYMicrosurgical Technology, Inc.K852032OCULAR PRESSURE REDUCER (MCCANNEL)Visitec Co.K840004WEE BAG O'MERCURYSurgi-Quip Inc.UK792255NEVYAS AUTOPRESS EYE COMPRESSORKeeler Optical Products , Ltd.

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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