LKB-BROMMA 2218 HISTORANGE MICROTOME
K-Number: K812157 · 1981-08-18
Device Summary
Frequently Asked Questions
What is the LKB-BROMMA 2218 HISTORANGE MICROTOME?
LKB-BROMMA 2218 HISTORANGE MICROTOME is a medical device that received FDA 510(k) clearance on 1981-08-18. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K812157.
When did LKB-BROMMA 2218 HISTORANGE MICROTOME receive FDA 510(k) clearance?
LKB-BROMMA 2218 HISTORANGE MICROTOME received FDA 510(k) clearance on 1981-08-18, under 510(k) number K812157.
Who is the listed applicant for LKB-BROMMA 2218 HISTORANGE MICROTOME?
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-BROMMA 2218 HISTORANGE MICROTOME?
The FDA product code for LKB-BROMMA 2218 HISTORANGE MICROTOME 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.