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510(k) FDA Premarket Notification K213391

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The following data is part of a premarket notification filed by with the FDA for .

Pre-market Notification Details

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Correspondent

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00840481134470 K213391 000
10840481132534 K213391 000
00840481109782 K213391 000
00840481122156 K213391 000
10840481132541 K213391 000
10840481132565 K213391 000
10840481132572 K213391 000
10840481132596 K213391 000
10840481132602 K213391 000
00840481132612 K213391 000
10840481132626 K213391 000
10840481132633 K213391 000
00840481132643 K213391 000
00840481132650 K213391 000
00840481132667 K213391 000
00840481134579 K213391 000

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Function: _error_handler

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