Citizen Watch Co., Ltd. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • No warning letters matched by name
Inspections 0 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 8 Latest Jun 26, 2006

Citizen Watch Co., Ltd. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Citizen Watch Co., Ltd." is on file.

What these totals cover: FDA records filed under the name "Citizen Watch Co., Ltd." and its spelling variant "Citizen Watch Co".

Latest 510(k)
Jun 26, 2006

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances8Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent 510(k) clearances

8 510(k) clearances from Oct 28, 1991 to Jun 26, 2006.

K-NumberDeviceDate
K061161BLOOD PRESSURE METER, MODEL CH-311BJun 26, 2006
K052046BLOOD PRESSURE METER, MODEL CH-432Oct 19, 2005
K001244BLOOD PRESSURE METER, MODELS CH-631B, CH-631D, CH-632B, CH-632DSep 26, 2000
K984223BLOOD PRESSURE METER, MODELS CH-491, CH-481, CH-471Apr 28, 1999
K973061CH-601A AND CH-601B DIGITAL WRIST SPHYGMOMANOMETER (CH-601A/CH-601B)Mar 13, 1998
K954547CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETERApr 1, 1997
K923344ELECTRONIC DIGITAL BLOOD PRESSURE MONITOROct 7, 1993
K911965ELECTRONIC DIGITAL BLOOD PRESSURE/PULSE MONITOROct 28, 1991

Citizen Watch Co., Ltd. and the FDA: common questions

Has Citizen Watch Co., Ltd. received an FDA warning letter?

No FDA warning letter addressed to the name "Citizen Watch Co., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Citizen Watch Co., Ltd. received an FDA Form 483?

FDA has not published a Form 483 for "Citizen Watch Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.