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FDA 510(k)

BIRT-A-SWITCH DSP #712

K-Number: K823491 · 1983-01-07

Decision Date1983-01-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIRT-A-SWITCH DSP #712 is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Corp.. It received FDA 510(k) clearance on 1983-01-07 under 510(k) number K823491. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIRT-A-SWITCH DSP #712?

BIRT-A-SWITCH DSP #712 is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is Birtcher Corp.. The 510(k) number is K823491.

When did BIRT-A-SWITCH DSP #712 receive FDA 510(k) clearance?

BIRT-A-SWITCH DSP #712 received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823491.

Who is the listed applicant for BIRT-A-SWITCH DSP #712?

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 #712?

The FDA product code for BIRT-A-SWITCH DSP #712 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.

View all 27 devices →

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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