BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768
K-Number: K860687 · 1986-03-24
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Device Summary
Frequently Asked Questions
What is the BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768?
BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768 is a medical device that received FDA 510(k) clearance on 1986-03-24. The listed applicant is Birtcher Corp.. The 510(k) number is K860687.
When did BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768 receive FDA 510(k) clearance?
BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768 received FDA 510(k) clearance on 1986-03-24, under 510(k) number K860687.
Who is the listed applicant for BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768?
The FDA 510(k) record lists Birtcher Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768?
The FDA product code for BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768 is GEI.
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 Birtcher Corp. 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: GEI)
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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