TENZCARE STIMULATOR 6890
K-Number: K891992 · 1989-10-12
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Device Summary
Frequently Asked Questions
What is the TENZCARE STIMULATOR 6890?
TENZCARE STIMULATOR 6890 is a medical device that received FDA 510(k) clearance on 1989-10-12. The listed applicant is 3M Company. The 510(k) number is K891992.
When did TENZCARE STIMULATOR 6890 receive FDA 510(k) clearance?
TENZCARE STIMULATOR 6890 received FDA 510(k) clearance on 1989-10-12, under 510(k) number K891992.
Who is the listed applicant for TENZCARE STIMULATOR 6890?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENZCARE STIMULATOR 6890?
The FDA product code for TENZCARE STIMULATOR 6890 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 3M Company 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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