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FDA 510(k)

THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER

K-Number: K884158 · 1989-01-17

ApplicantPpg Industries, Inc.
Decision Date1989-01-17
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Ppg Industries, Inc.. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K884158. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER?

THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Ppg Industries, Inc.. The 510(k) number is K884158.

When did THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER receive FDA 510(k) clearance?

THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER received FDA 510(k) clearance on 1989-01-17, under 510(k) number K884158.

Who is the listed applicant for THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER?

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

What is the FDA product code for THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER?

The FDA product code for THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER is CCK.

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Other records listing Ppg Industries, Inc. as applicant

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Related Devices (Code: CCK)

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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