FDA 510(k)
Substantially Equivalent
🇺🇸 United States
UNKNOWN
K Number: K827718
·
Decision Aug 16, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
7
Review Days
55
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- UNKNOWN
- K Number
- K827718
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Cranbury Medical Labs, Inc.
- Date Received
- June 22, 1982
- Decision Date
- August 16, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- RA
- Third Party
- N
Other Clearances by Cranbury Medical Labs, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K828586 | ENTREKIN MODEL DX-300 CONTINUOUS WAVE ULTRASONIC DOPPLER TRANSDUCER | Dec 14, 1982 | Substantially Equivalent |
| K822830 | MEDICAL LABS FETAL SCAN #1000 W/CENTRAL | Sep 30, 1982 | Substantially Equivalent |
| K827375 | BIOPSY GUIDE ATTACHMENT FOR USE WITH FETASCAN 2000 AND 2000A | Jul 2, 1982 | Substantially Equivalent |
| K827376 | BIOPSY GUIDE ATTACHMENT FOR USE WITH FETASCAN 800 | Jul 2, 1982 | Substantially Equivalent |
| K813457 | FETASCAN 2000,2000A OBSTETRICAL DATA | Feb 12, 1982 | Substantially Equivalent |
| K813458 | FETASCAN 1000, 1000A OBSTETRICAL DATA | Jan 28, 1982 | Substantially Equivalent |