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FDA 510(k)

SHORTWAVE DIATHERMY MODEL 802

K-Number: K780755 · 1978-05-12

ApplicantBirtcher Corp.
Decision Date1978-05-12
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SHORTWAVE DIATHERMY MODEL 802 is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Corp.. It received FDA 510(k) clearance on 1978-05-12 under 510(k) number K780755. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHORTWAVE DIATHERMY MODEL 802?

SHORTWAVE DIATHERMY MODEL 802 is a medical device that received FDA 510(k) clearance on 1978-05-12. The listed applicant is Birtcher Corp.. The 510(k) number is K780755.

When did SHORTWAVE DIATHERMY MODEL 802 receive FDA 510(k) clearance?

SHORTWAVE DIATHERMY MODEL 802 received FDA 510(k) clearance on 1978-05-12, under 510(k) number K780755.

Who is the listed applicant for SHORTWAVE DIATHERMY MODEL 802?

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 SHORTWAVE DIATHERMY MODEL 802?

The FDA product code for SHORTWAVE DIATHERMY MODEL 802 is IMJ.

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Other records listing Birtcher Corp. as applicant

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K881328MODEL 375 ECGK860718ELECTROSURGERY PENCIL, MODEL 767K860687BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768K854814SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33K854864BI-POLAR FORCEPSK850943MODEL 775 BIPOLAR COAGULATOR

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Related Devices (Code: IMJ)

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.

K252963BTL-899TTBTL Industries, Inc.K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLC

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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