HEMOGLOBINOMETER MODEL 720 B
FDA 510(k) clearance K781361 · decided 1978-09-14
Clearance details
- K-number
- K781361
- Device name
- HEMOGLOBINOMETER MODEL 720 B
- Applicant
- Innovative Medical Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1978-08-07
- Decision date
- 1978-09-14
- Days to decision
- 38 days
- Clearance type
- Traditional
- Product code
- GKR
- Device class
- 2
- Regulation number
- 864.5620
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| SHARPX NEEDLE DESTRUCTION UNIT (P980015/S005) | Innovative Medical Systems, Inc. | 2002-06-12 |
| SHARPX NEEDLE DESTRUCTION UNIT (P980015/S004) | Innovative Medical Systems, Inc. | 2001-08-15 |
| SHARP(X)TM NEEDLE DESTRUCTION UNIT (P980015/S003) | Innovative Medical Systems, Inc. | 1999-09-17 |
| SHARP NEEDLE DESTRUCTION UNIT (P980015/S002) | Innovative Medical Systems, Inc. | 1999-03-19 |
| SHARP NEEDLE DESTRUCTION UNIT (P980015/S001) | Innovative Medical Systems, Inc. | 1998-12-14 |
| SHARPX (P980015) | Innovative Medical Systems, Inc. | 1998-08-06 |