510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850740Substantially Equivalent

Sechrist Volume Ventilator Modification

Sechrist Industries Inc, Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850740 is the FDA 510(k) clearance record for SECHRIST VOLUME VENTILATOR MODIFICATION, cleared for Sechrist Industries, Inc. on . FDA records list 23 510(k) clearances for Sechrist Industries, Inc., from to . As of , FDA records show no recalls naming K850740.

Clearance record

Decision date
Received
(182 days to decision)
Review panel
Unknown
Applicant
Sechrist Industries, Inc. 2820 Gretta Ln., Anaheim CA
Third party review
No