FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2
K Number: K861890
·
Decision Jun 3, 1986
Classifications
1
FEI Numbers
258
Registration Numbers
258
Same Product Code
15
Applicant Total
33
Review Days
18
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Basic Information
- Device Name
- 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2
- K Number
- K861890
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.4010
- Medical Specialty
- Pathology
- Decision
- Substantially Equivalent
- Applicant
- Richard-Allan Medical Ind., Inc.
- Date Received
- May 16, 1986
- Decision Date
- June 3, 1986
- Product Code
- PPM
- Advisory Committee
- Pathology
- Review Advisory Committee
- PA
- 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 |
|---|---|---|---|
| PPM | General Purpose Reagent | FDA class 1 | Pathology |
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Other Clearances by Richard-Allan Medical Ind., Inc.
| K Number | Device Name | ||
|---|---|---|---|
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| K924761 | STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD | Apr 20, 1993 | Substantially Equivalent |
| K900566 | RICHARD-ALLAN VESSEL LOOPS | May 3, 1990 | Substantially Equivalent |
| K896262 | TITANIUM LIGATING CLIPS | Jan 2, 1990 | Substantially Equivalent |
| K890314 | PROTECTOR (SURGICAL INSTRUMENT) | Feb 27, 1989 | Substantially Equivalent |
| K873309 | REFLEX(TM) CA-T CLIP APPLIER | Nov 27, 1987 | Substantially Equivalent |
| K862404 | REFLEX(TM) CLIP APPLIER | Jul 23, 1986 | Substantially Equivalent |
| K862223 | MICRO THIN* PARAFFIN | Jun 17, 1986 | Substantially Equivalent |