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FDA 510(k)

RE-CELL SLIDE RECAP

K-Number: K772139 · 1978-01-05

ApplicantGeometric Data, Div. Smithkline Corp.
Decision Date1978-01-05
Product CodeJOY
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RE-CELL SLIDE RECAP is the device name listed in this FDA 510(k) record. The listed applicant is Geometric Data, Div. Smithkline Corp.. It received FDA 510(k) clearance on 1978-01-05 under 510(k) number K772139. The device is classified under product code JOY. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RE-CELL SLIDE RECAP?

RE-CELL SLIDE RECAP is a medical device that received FDA 510(k) clearance on 1978-01-05. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K772139.

When did RE-CELL SLIDE RECAP receive FDA 510(k) clearance?

RE-CELL SLIDE RECAP received FDA 510(k) clearance on 1978-01-05, under 510(k) number K772139.

Who is the listed applicant for RE-CELL SLIDE RECAP?

The FDA 510(k) record lists Geometric Data, Div. Smithkline Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RE-CELL SLIDE RECAP?

The FDA product code for RE-CELL SLIDE RECAP is JOY.

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Other records listing Geometric Data, Div. Smithkline Corp. 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.

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