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FDA 510(k)

TPC-LYOPHILIZED POOLED HUMAN PLASMA

K-Number: K761091 · 1977-02-01

ApplicantBio/Data Corp.
Decision Date1977-02-01
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TPC-LYOPHILIZED POOLED HUMAN PLASMA is the device name listed in this FDA 510(k) record. The listed applicant is Bio/Data Corp.. It received FDA 510(k) clearance on 1977-02-01 under 510(k) number K761091. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TPC-LYOPHILIZED POOLED HUMAN PLASMA?

TPC-LYOPHILIZED POOLED HUMAN PLASMA is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is Bio/Data Corp.. The 510(k) number is K761091.

When did TPC-LYOPHILIZED POOLED HUMAN PLASMA receive FDA 510(k) clearance?

TPC-LYOPHILIZED POOLED HUMAN PLASMA received FDA 510(k) clearance on 1977-02-01, under 510(k) number K761091.

Who is the listed applicant for TPC-LYOPHILIZED POOLED HUMAN PLASMA?

The FDA 510(k) record lists Bio/Data Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TPC-LYOPHILIZED POOLED HUMAN PLASMA?

The FDA product code for TPC-LYOPHILIZED POOLED HUMAN PLASMA is JPA.

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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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