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FDA 510(k)

SOLUBLE COLLAGEN

K-Number: K780285 · 1978-03-30

ApplicantGeneral Diagnostics
Decision Date1978-03-30
Product CodeJOZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SOLUBLE COLLAGEN is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1978-03-30 under 510(k) number K780285. The device is classified under product code JOZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLUBLE COLLAGEN?

SOLUBLE COLLAGEN is a medical device that received FDA 510(k) clearance on 1978-03-30. The listed applicant is General Diagnostics. The 510(k) number is K780285.

When did SOLUBLE COLLAGEN receive FDA 510(k) clearance?

SOLUBLE COLLAGEN received FDA 510(k) clearance on 1978-03-30, under 510(k) number K780285.

Who is the listed applicant for SOLUBLE COLLAGEN?

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

What is the FDA product code for SOLUBLE COLLAGEN?

The FDA product code for SOLUBLE COLLAGEN is JOZ.

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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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