FDA 510(k)

TRANSFORMER

K-Number: K822267 · 1982-10-13

Decision Date1982-10-13

Product Code

DecisionSubstantially Equivalent

Device Summary

TRANSFORMER is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-10-13 under 510(k) number K822267. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSFORMER?

TRANSFORMER is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Kelleher Corp.. The 510(k) number is K822267.

When did TRANSFORMER receive FDA 510(k) clearance?

TRANSFORMER received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822267.

Who is the listed applicant for TRANSFORMER?

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

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Other records listing Kelleher Corp. as applicant

K822618EMERGENCY TRACHEOSTOMY INSTRUMENT SET K822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH K823083ELECTROSURGICAL UNIT K822252ENT TREATMENT UNITS K823111NYSTYMOGRAPH ACCESS K822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS

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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.