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FDA 510(k)

EXTENSION/OSCILLATOR TABLE

K-Number: K870427 · 1987-02-13

ApplicantHeidelberg Medical Products
Decision Date1987-02-13
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EXTENSION/OSCILLATOR TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Heidelberg Medical Products. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K870427. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSION/OSCILLATOR TABLE?

EXTENSION/OSCILLATOR TABLE is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Heidelberg Medical Products. The 510(k) number is K870427.

When did EXTENSION/OSCILLATOR TABLE receive FDA 510(k) clearance?

EXTENSION/OSCILLATOR TABLE received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870427.

Who is the listed applicant for EXTENSION/OSCILLATOR TABLE?

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

What is the FDA product code for EXTENSION/OSCILLATOR TABLE?

The FDA product code for EXTENSION/OSCILLATOR TABLE is JFB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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