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FDA 510(k)

BIRT-A-PAD #730

K-Number: K823492 · 1982-12-09

ApplicantBirtcher Corp.
Decision Date1982-12-09
Product Code
DecisionSubstantially Equivalent

Device Summary

BIRT-A-PAD #730 is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Corp.. It received FDA 510(k) clearance on 1982-12-09 under 510(k) number K823492. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIRT-A-PAD #730?

BIRT-A-PAD #730 is a medical device that received FDA 510(k) clearance on 1982-12-09. The listed applicant is Birtcher Corp.. The 510(k) number is K823492.

When did BIRT-A-PAD #730 receive FDA 510(k) clearance?

BIRT-A-PAD #730 received FDA 510(k) clearance on 1982-12-09, under 510(k) number K823492.

Who is the listed applicant for BIRT-A-PAD #730?

The FDA 510(k) record lists Birtcher Corp. as the applicant. This does not by itself establish the device manufacturer.

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.

K881328MODEL 375 ECGK860687BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768K860718ELECTROSURGERY PENCIL, MODEL 767K854814SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33K854864BI-POLAR FORCEPSK850943MODEL 775 BIPOLAR COAGULATOR

View all 27 devices →

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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