MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR
K-Number: K871666 · 1987-06-25
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Device Summary
Frequently Asked Questions
What is the MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR?
MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR is a medical device that received FDA 510(k) clearance on 1987-06-25. The listed applicant is Oriental Medical Supplies, Inc.. The 510(k) number is K871666.
When did MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR receive FDA 510(k) clearance?
MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR received FDA 510(k) clearance on 1987-06-25, under 510(k) number K871666.
Who is the listed applicant for MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR?
The FDA 510(k) record lists Oriental Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR?
The FDA product code for MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR is GZJ.
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 Oriental Medical Supplies, 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: GZJ)
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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