PRO-TEC-CASE
K-Number: K950530 · 1995-04-07
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Device Summary
Frequently Asked Questions
What is the PRO-TEC-CASE?
PRO-TEC-CASE is a medical device that received FDA 510(k) clearance on 1995-04-07. The listed applicant is Hyman, Phelps & McNamara, P.C.. The 510(k) number is K950530.
When did PRO-TEC-CASE receive FDA 510(k) clearance?
PRO-TEC-CASE received FDA 510(k) clearance on 1995-04-07, under 510(k) number K950530.
Who is the listed applicant for PRO-TEC-CASE?
The FDA 510(k) record lists Hyman, Phelps & McNamara, P.C. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRO-TEC-CASE?
The FDA product code for PRO-TEC-CASE is LRX.
Other records listing Hyman, Phelps & McNamara, P.C. 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: LRX)
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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