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FDA 510(k)

PERKINELMER 226 SAMPLE COLLECTION DEVICES

K-Number: K121864 · 2013-03-12

ApplicantPerkinelmer, Inc.
Decision Date2013-03-12
Product CodePJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PERKINELMER 226 SAMPLE COLLECTION DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Perkinelmer, Inc.. It received FDA 510(k) clearance on 2013-03-12 under 510(k) number K121864. The device is classified under product code PJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERKINELMER 226 SAMPLE COLLECTION DEVICES?

PERKINELMER 226 SAMPLE COLLECTION DEVICES is a medical device that received FDA 510(k) clearance on 2013-03-12. The listed applicant is Perkinelmer, Inc.. The 510(k) number is K121864.

When did PERKINELMER 226 SAMPLE COLLECTION DEVICES receive FDA 510(k) clearance?

PERKINELMER 226 SAMPLE COLLECTION DEVICES received FDA 510(k) clearance on 2013-03-12, under 510(k) number K121864.

Who is the listed applicant for PERKINELMER 226 SAMPLE COLLECTION DEVICES?

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

What is the FDA product code for PERKINELMER 226 SAMPLE COLLECTION DEVICES?

The FDA product code for PERKINELMER 226 SAMPLE COLLECTION DEVICES is PJC.

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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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