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FDA 510(k)

STRYKER PEEK TWINLOOP TAC

K-Number: K070882 · 2007-07-20

ApplicantStryker Endoscopy
Decision Date2007-07-20
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER PEEK TWINLOOP TAC is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2007-07-20 under 510(k) number K070882. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER PEEK TWINLOOP TAC?

STRYKER PEEK TWINLOOP TAC is a medical device that received FDA 510(k) clearance on 2007-07-20. The listed applicant is Stryker Endoscopy. The 510(k) number is K070882.

When did STRYKER PEEK TWINLOOP TAC receive FDA 510(k) clearance?

STRYKER PEEK TWINLOOP TAC received FDA 510(k) clearance on 2007-07-20, under 510(k) number K070882.

Who is the listed applicant for STRYKER PEEK TWINLOOP TAC?

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

What is the FDA product code for STRYKER PEEK TWINLOOP TAC?

The FDA product code for STRYKER PEEK TWINLOOP TAC is MBI.

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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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