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FDA 510(k)

SYS*STIM 208 AND 208A

K-Number: K031017 · 2003-05-30

Decision Date2003-05-30
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SYS*STIM 208 AND 208A is the device name listed in this FDA 510(k) record. The listed applicant is Mettler Electronics Corp.. It received FDA 510(k) clearance on 2003-05-30 under 510(k) number K031017. 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 SYS*STIM 208 AND 208A?

SYS*STIM 208 AND 208A is a medical device that received FDA 510(k) clearance on 2003-05-30. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K031017.

When did SYS*STIM 208 AND 208A receive FDA 510(k) clearance?

SYS*STIM 208 AND 208A received FDA 510(k) clearance on 2003-05-30, under 510(k) number K031017.

Who is the listed applicant for SYS*STIM 208 AND 208A?

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

What is the FDA product code for SYS*STIM 208 AND 208A?

The FDA product code for SYS*STIM 208 AND 208A is IPF.

Other records listing Mettler Electronics 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.

View all 32 devices →

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.

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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