FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
MODIFICATION OF BIONECT CLEAR HYDROGEL
K Number: K984264
·
Decision Feb 10, 1999
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
144
Applicant Total
10
Review Days
85
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Basic Information
- Device Name
- MODIFICATION OF BIONECT CLEAR HYDROGEL
- K Number
- K984264
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Fidia Pharmaceutical Corp.
- Date Received
- November 17, 1998
- Decision Date
- February 10, 1999
- Product Code
- MGQ
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | FDA unclassified | Unknown |
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TENDERWET ACTIVE
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Other Clearances by Fidia Pharmaceutical Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K984266 | MODIFICATION OF BIONECT HYDROGEL SPRAY | Feb 10, 1999 | Substantially Equivalent |
| K984413 | BIONECT HYDROGEL | Feb 10, 1999 | Substantially Equivalent |
| K984262 | MODIFICATION OF BIONECT HYDROGEL GAUZE PADS | Feb 10, 1999 | Substantially Equivalent |
| K984267 | MODIFICATION OF BIONECT HYDROGEL FOAM | Feb 10, 1999 | Substantially Equivalent |
| K973725 | BIONECT CLEAR HYDROGEL | Sep 22, 1998 | Substantially Equivalent |
| K973721 | BIONECT HYDROGEL GAUZE PADS | Sep 22, 1998 | Substantially Equivalent |
| K973722 | BIONECT HYDROGEL FOAM | Sep 22, 1998 | Substantially Equivalent |
| K973724 | BIONECT HYDROGEL SPRAY | Sep 22, 1998 | Substantially Equivalent |
| K963004 | BIONECT CREAM | Feb 12, 1997 | Substantially Equivalent for Some Indications |