APL SIM MEDIUM
K-Number: K853618 · 1985-09-16
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Device Summary
Frequently Asked Questions
What is the APL SIM MEDIUM?
APL SIM MEDIUM is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Apl Medical Supplies. The 510(k) number is K853618.
When did APL SIM MEDIUM receive FDA 510(k) clearance?
APL SIM MEDIUM received FDA 510(k) clearance on 1985-09-16, under 510(k) number K853618.
Who is the listed applicant for APL SIM MEDIUM?
The FDA 510(k) record lists Apl Medical Supplies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APL SIM MEDIUM?
The FDA product code for APL SIM MEDIUM is JSH.
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 Apl Medical Supplies 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: JSH)
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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