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FDA 510(k)

AFTER LOADING BUCHLER

K-Number: K832789 · 1983-09-29

ApplicantEllis Pharmaceutical Consulting, Inc.
Decision Date1983-09-29
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AFTER LOADING BUCHLER is the device name listed in this FDA 510(k) record. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832789. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFTER LOADING BUCHLER?

AFTER LOADING BUCHLER is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. The 510(k) number is K832789.

When did AFTER LOADING BUCHLER receive FDA 510(k) clearance?

AFTER LOADING BUCHLER received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832789.

Who is the listed applicant for AFTER LOADING BUCHLER?

The FDA 510(k) record lists Ellis Pharmaceutical Consulting, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AFTER LOADING BUCHLER?

The FDA product code for AFTER LOADING BUCHLER is JAQ.

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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.

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