FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MSI 3002 SERIES BED
K Number: K881963
·
Decision Jun 28, 1988
Classifications
1
FEI Numbers
228
Registration Numbers
228
Same Product Code
69
Applicant Total
9
Review Days
49
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Basic Information
- Device Name
- MSI 3002 SERIES BED
- K Number
- K881963
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5100
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Med Service, Inc.
- Date Received
- May 10, 1988
- Decision Date
- June 28, 1988
- Product Code
- FNL
- 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 |
|---|---|---|---|
| FNL | Bed, Ac-Powered Adjustable Hospital | FDA class 2 | General Hospital |
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Other Clearances by Med Service, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K881961 | MSI STANDARD BED MODELS: L1097-64 AND L1085-64 | Nov 1, 1988 | Substantially Equivalent |
| K881960 | MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74 | Nov 1, 1988 | Substantially Equivalent |
| K881782 | MSI 4000 SERIES BED | Jul 12, 1988 | Substantially Equivalent |
| K881964 | MSI 3003 SERIES BED | Jun 28, 1988 | Substantially Equivalent |
| K881962 | MSI 2005 SERIES BED | Jun 3, 1988 | Substantially Equivalent |
| K881965 | MSI 5000 SERIES BED | May 31, 1988 | Substantially Equivalent |
| K881027 | MSI 2002 SERIES BED | May 26, 1988 | Substantially Equivalent |
| K873291 | MSI 9000 SERIES BED | Dec 30, 1987 | Substantially Equivalent |