FDA 510(k)

NEGATIVE CONTROL SERUM

K-Number: K760836 · 1976-11-01

Decision Date1976-11-01

Product Code

DecisionSubstantially Equivalent

Device Summary

NEGATIVE CONTROL SERUM is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760836. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEGATIVE CONTROL SERUM?

NEGATIVE CONTROL SERUM is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is I M, Inc.. The 510(k) number is K760836.

When did NEGATIVE CONTROL SERUM receive FDA 510(k) clearance?

NEGATIVE CONTROL SERUM received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760836.

Who is the listed applicant for NEGATIVE CONTROL SERUM?

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

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 I M, Inc. as applicant

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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.