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FDA 510(k)

LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM

K-Number: K872369 · 1988-02-22

ApplicantLoma Linda University Medical Center
Decision Date1988-02-22
Product CodeIWM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Loma Linda University Medical Center. It received FDA 510(k) clearance on 1988-02-22 under 510(k) number K872369. The device is classified under product code IWM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM?

LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is Loma Linda University Medical Center. The 510(k) number is K872369.

When did LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM receive FDA 510(k) clearance?

LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM received FDA 510(k) clearance on 1988-02-22, under 510(k) number K872369.

Who is the listed applicant for LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM?

The FDA 510(k) record lists Loma Linda University Medical Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM?

The FDA product code for LOMA LINDA UNIV. PROTON BEAM THERAPY SYSTEM is IWM.

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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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