PALCO LABS LOADMATIC
K-Number: K913694 · 1991-12-17
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Device Summary
Frequently Asked Questions
What is the PALCO LABS LOADMATIC?
PALCO LABS LOADMATIC is a medical device that received FDA 510(k) clearance on 1991-12-17. The listed applicant is Palco Laboratories, Inc.. The 510(k) number is K913694.
When did PALCO LABS LOADMATIC receive FDA 510(k) clearance?
PALCO LABS LOADMATIC received FDA 510(k) clearance on 1991-12-17, under 510(k) number K913694.
Who is the listed applicant for PALCO LABS LOADMATIC?
The FDA 510(k) record lists Palco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PALCO LABS LOADMATIC?
The FDA product code for PALCO LABS LOADMATIC is FMF.
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 Palco Laboratories, 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: FMF)
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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