FDA 510(k)

PELLET, CALIBRATION

K-Number: K770172 · 1977-02-07

Decision Date1977-02-07

Product Code

DecisionSubstantially Equivalent

Device Summary

PELLET, CALIBRATION is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1977-02-07 under 510(k) number K770172. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PELLET, CALIBRATION?

PELLET, CALIBRATION is a medical device that received FDA 510(k) clearance on 1977-02-07. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K770172.

When did PELLET, CALIBRATION receive FDA 510(k) clearance?

PELLET, CALIBRATION received FDA 510(k) clearance on 1977-02-07, under 510(k) number K770172.

Who is the listed applicant for PELLET, CALIBRATION?

The FDA 510(k) record lists Deringer-Ney, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Deringer-Ney, Inc. as applicant

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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.