SECHRIST VOLUME VENTILATOR MODIFICATION
FDA 510(k) clearance K850740 · decided 1985-07-29
Clearance details
- K-number
- K850740
- Device name
- SECHRIST VOLUME VENTILATOR MODIFICATION
- Applicant
- Sechrist Industries, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1985-01-28
- Decision date
- 1985-07-29
- Days to decision
- 182 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Anaheim, CA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Sechrist Industries
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Recalls involving this device
No recalls on record reference this clearance.