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FDA 510(k)

MULTIPLE

K-Number: K933616 · 1993-09-20

Decision Date1993-09-20
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTIPLE is the device name listed in this FDA 510(k) record. The listed applicant is Greg and Greg, Inc.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K933616. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE?

MULTIPLE is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Greg and Greg, Inc.. The 510(k) number is K933616.

When did MULTIPLE receive FDA 510(k) clearance?

MULTIPLE received FDA 510(k) clearance on 1993-09-20, under 510(k) number K933616.

Who is the listed applicant for MULTIPLE?

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

What is the FDA product code for MULTIPLE?

The FDA product code for MULTIPLE is HQY.

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.

Related PubMed Literature

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.

Related Devices (Code: HQY)

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

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