MASTERLAB PFT AND MASTERLAB BODY BOX
FDA 510(k) clearance K893420 · decided 1989-06-23
Clearance details
- K-number
- K893420
- Device name
- MASTERLAB PFT AND MASTERLAB BODY BOX
- Applicant
- Quinton, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-04-27
- Decision date
- 1989-06-23
- Days to decision
- 57 days
- Clearance type
- Traditional
- Product code
- CCM
- Device class
- 2
- Regulation number
- 868.1750
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Seattle, WA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Quinton
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.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| MASTERSCREEN PAED - BABY BODY (K081823) | Viasys Healthcare GmbH | 2009-05-18 |
| MS PAED-BABY BODY (K023796) | Erich Jaeger GmbH | 2003-03-03 |
| 1085 ULTIMATE E PLETHYSMOGRAPH (K943259) | Medical Graphics Corp. | 1995-04-10 |
| INFANT BODY TEST (K853390) | Erich Jaeger, Inc. | 1986-02-05 |
| COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM (K852102) | Warren E. Collins, Inc. | 1985-07-31 |
| SYSTEM 1085 BODY PLETHYSMOGRAPH (K852088) | Medical Graphics Corp. | 1985-07-30 |
| UNIVERSAL-BODYTEST (K843846) | Erich Jaeger, Inc. | 1985-02-14 |
| BODYSCREEN II (K843851) | Erich Jaeger, Inc. | 1985-02-14 |
| 4200 PNEUMATIC MOUTH SHUTTER (K791705) | Hans Rudolph, Inc. | 1979-10-04 |
| CHEST BELLOWS, SMALL (K772367) | Honeywell, Inc. | 1978-01-11 |
Recalls involving this device
No recalls on record reference this clearance.