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FDA 510(k)

CELL COUNTING GRID GRATICULE

K-Number: K874190 · 1988-01-05

Decision Date1988-01-05
Product CodeIBJ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CELL COUNTING GRID GRATICULE is the device name listed in this FDA 510(k) record. The listed applicant is Portable Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1988-01-05 under 510(k) number K874190. The device is classified under product code IBJ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CELL COUNTING GRID GRATICULE?

CELL COUNTING GRID GRATICULE is a medical device that received FDA 510(k) clearance on 1988-01-05. The listed applicant is Portable Medical Laboratories, Inc.. The 510(k) number is K874190.

When did CELL COUNTING GRID GRATICULE receive FDA 510(k) clearance?

CELL COUNTING GRID GRATICULE received FDA 510(k) clearance on 1988-01-05, under 510(k) number K874190.

Who is the listed applicant for CELL COUNTING GRID GRATICULE?

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

What is the FDA product code for CELL COUNTING GRID GRATICULE?

The FDA product code for CELL COUNTING GRID GRATICULE is IBJ.

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.

Other records listing Portable Medical Laboratories, Inc. 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.

View all 9 devices →

Related Devices (Code: IBJ)

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.

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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