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FDA 510(k)

S*E*M*M-SET & C*U*R*T-SET

K-Number: K932617 · 1994-03-07

ApplicantMarket-Tiers, Inc.
Decision Date1994-03-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

S*E*M*M-SET & C*U*R*T-SET is the device name listed in this FDA 510(k) record. The listed applicant is Market-Tiers, Inc.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K932617. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S*E*M*M-SET & C*U*R*T-SET?

S*E*M*M-SET & C*U*R*T-SET is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Market-Tiers, Inc.. The 510(k) number is K932617.

When did S*E*M*M-SET & C*U*R*T-SET receive FDA 510(k) clearance?

S*E*M*M-SET & C*U*R*T-SET received FDA 510(k) clearance on 1994-03-07, under 510(k) number K932617.

Who is the listed applicant for S*E*M*M-SET & C*U*R*T-SET?

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

What is the FDA product code for S*E*M*M-SET & C*U*R*T-SET?

The FDA product code for S*E*M*M-SET & C*U*R*T-SET is GCJ.

Related Devices (Code: GCJ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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