LKB 2260 MACROTOME
K-Number: K864733 · 1987-01-05
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Device Summary
Frequently Asked Questions
What is the LKB 2260 MACROTOME?
LKB 2260 MACROTOME is a medical device that received FDA 510(k) clearance on 1987-01-05. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K864733.
When did LKB 2260 MACROTOME receive FDA 510(k) clearance?
LKB 2260 MACROTOME received FDA 510(k) clearance on 1987-01-05, under 510(k) number K864733.
Who is the listed applicant for LKB 2260 MACROTOME?
The FDA 510(k) record lists Lkb Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LKB 2260 MACROTOME?
The FDA product code for LKB 2260 MACROTOME is IDO.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Lkb Instruments, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IDO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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