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FDA 510(k)

EPPENDORF PCP 6121

K-Number: K781544 · 1978-10-03

ApplicantMarilyn L. Amick
Decision Date1978-10-03
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EPPENDORF PCP 6121 is the device name listed in this FDA 510(k) record. The listed applicant is Marilyn L. Amick. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K781544. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPPENDORF PCP 6121?

EPPENDORF PCP 6121 is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Marilyn L. Amick. The 510(k) number is K781544.

When did EPPENDORF PCP 6121 receive FDA 510(k) clearance?

EPPENDORF PCP 6121 received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781544.

Who is the listed applicant for EPPENDORF PCP 6121?

The FDA 510(k) record lists Marilyn L. Amick as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPPENDORF PCP 6121?

The FDA product code for EPPENDORF PCP 6121 is JJQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Marilyn L. Amick as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K802568HEMOGLOBIN CONTROLK802569ABNORMAL HEMOGLOBIN CONTROL

Related Devices (Code: JJQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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