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FDA 510(k)

RICH-MAR G1000 EMS

K-Number: K880948 · 1988-04-21

ApplicantRich-Mar Corp.
Decision Date1988-04-21
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RICH-MAR G1000 EMS is the device name listed in this FDA 510(k) record. The listed applicant is Rich-Mar Corp.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K880948. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICH-MAR G1000 EMS?

RICH-MAR G1000 EMS is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Rich-Mar Corp.. The 510(k) number is K880948.

When did RICH-MAR G1000 EMS receive FDA 510(k) clearance?

RICH-MAR G1000 EMS received FDA 510(k) clearance on 1988-04-21, under 510(k) number K880948.

Who is the listed applicant for RICH-MAR G1000 EMS?

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

What is the FDA product code for RICH-MAR G1000 EMS?

The FDA product code for RICH-MAR G1000 EMS is IPF.

Other records listing Rich-Mar 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.

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Related Devices (Code: IPF)

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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