FDA 510(k)

PARALLEL-A-PREP

K-Number: K801853 · 1980-08-13

Decision Date1980-08-13

Product CodeEGI

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PARALLEL-A-PREP is the device name listed in this FDA 510(k) record. The listed applicant is C.D. Charles, Inc.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801853. The device is classified under product code EGI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARALLEL-A-PREP?

PARALLEL-A-PREP is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is C.D. Charles, Inc.. The 510(k) number is K801853.

When did PARALLEL-A-PREP receive FDA 510(k) clearance?

PARALLEL-A-PREP received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801853.

Who is the listed applicant for PARALLEL-A-PREP?

The FDA 510(k) record lists C.D. Charles, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARALLEL-A-PREP?

The FDA product code for PARALLEL-A-PREP is EGI.

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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.