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FDA 510(k)

CHECK-MATE AND CHECK-MATE [+]

K-Number: K871359 · 1987-05-29

ApplicantVeritech, Inc.
Decision Date1987-05-29
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHECK-MATE AND CHECK-MATE [+] is the device name listed in this FDA 510(k) record. The listed applicant is Veritech, Inc.. It received FDA 510(k) clearance on 1987-05-29 under 510(k) number K871359. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHECK-MATE AND CHECK-MATE [+]?

CHECK-MATE AND CHECK-MATE [+] is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is Veritech, Inc.. The 510(k) number is K871359.

When did CHECK-MATE AND CHECK-MATE [+] receive FDA 510(k) clearance?

CHECK-MATE AND CHECK-MATE [+] received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871359.

Who is the listed applicant for CHECK-MATE AND CHECK-MATE [+]?

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

What is the FDA product code for CHECK-MATE AND CHECK-MATE [+]?

The FDA product code for CHECK-MATE AND CHECK-MATE [+] is EFW.

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Related Devices (Code: EFW)

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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