FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
COLONGLIDE(R) LUBRICANT
K Number: K131617
·
Decision Oct 3, 2013
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
48
Applicant Total
2
Review Days
122
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Basic Information
- Device Name
- COLONGLIDE(R) LUBRICANT
- K Number
- K131617
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6375
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Pediatric Pharmaceuticals, Inc.
- Date Received
- June 3, 2013
- Decision Date
- October 3, 2013
- Product Code
- KMJ
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| KMJ | Lubricant, Patient | FDA class 1 | General Hospital |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KMJ), ordered by most recent decision date.
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Other Clearances by Pediatric Pharmaceuticals, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K141028 | COLONGLIDE LUBRICANT | Jul 24, 2014 | Substantially Equivalent |