CHESHIRE
K-Number: K952778 · 1995-09-06
Advertisement
Device Summary
Frequently Asked Questions
What is the CHESHIRE?
CHESHIRE is a medical device that received FDA 510(k) clearance on 1995-09-06. The listed applicant is Perceptive Systems, Inc.. The 510(k) number is K952778.
When did CHESHIRE receive FDA 510(k) clearance?
CHESHIRE received FDA 510(k) clearance on 1995-09-06, under 510(k) number K952778.
Who is the listed applicant for CHESHIRE?
The FDA 510(k) record lists Perceptive Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHESHIRE?
The FDA product code for CHESHIRE is LLZ.
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 Perceptive Systems, 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: LLZ)
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.
Advertisement