510(k) K895588
K895588 is an FDA 510(k) premarket notification submitted by Life Sciences Manufacturing, Inc. for the device "PORTABLE AIR PLETHYSMOGRAPH". The FDA issued a decision of Substantially Equivalent on March 27, 1990. The device falls under product code DSB (Plethysmograph, Impedance), a Class II device regulated under 21 CFR 870.2770. Life Sciences Manufacturing, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 27, 1990
- Date Received
- September 15, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plethysmograph, Impedance
- Device Class
- Class II
- Regulation Number
- 870.2770
- Review Panel
- CV
- Submission Type