LKB-BROMMA 2218 HISTORANGE MICROTOME
FDA 510(k) clearance K812157 · decided 1981-08-18
Clearance details
- K-number
- K812157
- Device name
- LKB-BROMMA 2218 HISTORANGE MICROTOME
- Applicant
- Lkb Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1981-07-29
- Decision date
- 1981-08-18
- Days to decision
- 20 days
- Clearance type
- Traditional
- Product code
- IDO
- Device class
- 1
- Regulation number
- 864.3010
- Medical specialty
- Pathology
- Advisory committee
- Pathology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Lkb Instruments
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| LKB 2260 MACROTOME (K864733) | Lkb Instruments, Inc. | 1987-01-05 |
| ROTARY MICROTOME (K863548) | Surgipath Medical Industries, Inc. | 1986-09-19 |
| LKB 2230 ROTARY ONE (K843505) | Lkb Instruments, Inc. | 1984-11-30 |
| TISSUE-TEK III ACCU-CUT ROTARY MICROTOME (K812558) | Miles Laboratories, Inc. | 1981-09-29 |
Recalls involving this device
No recalls on record reference this clearance.