TALLEY SD.500 SKIN PRESSURE EVALUATOR
K-Number: K914780 · 1991-12-19
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Device Summary
Frequently Asked Questions
What is the TALLEY SD.500 SKIN PRESSURE EVALUATOR?
TALLEY SD.500 SKIN PRESSURE EVALUATOR is a medical device that received FDA 510(k) clearance on 1991-12-19. The listed applicant is Talley Group, Ltd.. The 510(k) number is K914780.
When did TALLEY SD.500 SKIN PRESSURE EVALUATOR receive FDA 510(k) clearance?
TALLEY SD.500 SKIN PRESSURE EVALUATOR received FDA 510(k) clearance on 1991-12-19, under 510(k) number K914780.
Who is the listed applicant for TALLEY SD.500 SKIN PRESSURE EVALUATOR?
The FDA 510(k) record lists Talley Group, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TALLEY SD.500 SKIN PRESSURE EVALUATOR?
The FDA product code for TALLEY SD.500 SKIN PRESSURE EVALUATOR is IKE.
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 Talley Group, Ltd. 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: IKE)
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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