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FDA 510(k)

CAP-MOBILE

K-Number: K781425 · 1978-09-11

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1978-09-11
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAP-MOBILE is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1978-09-11 under 510(k) number K781425. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP-MOBILE?

CAP-MOBILE is a medical device that received FDA 510(k) clearance on 1978-09-11. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K781425.

When did CAP-MOBILE receive FDA 510(k) clearance?

CAP-MOBILE received FDA 510(k) clearance on 1978-09-11, under 510(k) number K781425.

Who is the listed applicant for CAP-MOBILE?

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

What is the FDA product code for CAP-MOBILE?

The FDA product code for CAP-MOBILE is IZL.

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Related Devices (Code: IZL)

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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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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