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FDA 510(k)

MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES

K-Number: K900316 · 1990-04-16

ApplicantIrvine Scientific
Decision Date1990-04-16
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Scientific. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K900316. The device is classified under product code HDR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES?

MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Irvine Scientific. The 510(k) number is K900316.

When did MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES receive FDA 510(k) clearance?

MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES received FDA 510(k) clearance on 1990-04-16, under 510(k) number K900316.

Who is the listed applicant for MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES?

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

What is the FDA product code for MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES?

The FDA product code for MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES is HDR.

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Other records listing Irvine Scientific 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.

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Related Devices (Code: HDR)

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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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