FDA 510(k)
Substantially Equivalent
🇺🇸 United States
WESCOTT TYPE BIOPSY NEEDLE
K Number: K842406
·
Decision Aug 9, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
8
Review Days
51
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Basic Information
- Device Name
- WESCOTT TYPE BIOPSY NEEDLE
- K Number
- K842406
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Popper & Sons, Inc.
- Date Received
- June 19, 1984
- Decision Date
- August 9, 1984
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- Third Party
- N
Other Clearances by Popper & Sons, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K911397 | HYPODERMIC NEEDLES, SINGLE LUMEN | May 20, 1991 | Substantially Equivalent |
| K843830 | J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI | Oct 26, 1984 | Substantially Equivalent |
| K843690 | ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE | Oct 25, 1984 | Substantially Equivalent |
| K841300 | ANTRUM NEEDLE-WOLF TYPE | Jun 5, 1984 | Substantially Equivalent |
| K841301 | GARDNER TYPE BONE MARROW NEEDLE | Jun 5, 1984 | Substantially Equivalent |
| K841299 | BIERMAN BIOPSY NEEDLE | May 2, 1984 | Substantially Equivalent |
| K840168 | WESTERMAN-JENSEN BIOPSY NEEDLE | Mar 12, 1984 | Substantially Equivalent |