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FDA 510(k)

DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS

K-Number: K963955 · 1996-11-19

ApplicantBert & Joe'S, Inc.
Decision Date1996-11-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS is the device name listed in this FDA 510(k) record. The listed applicant is Bert & Joe'S, Inc.. It received FDA 510(k) clearance on 1996-11-19 under 510(k) number K963955. 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 DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS?

DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS is a medical device that received FDA 510(k) clearance on 1996-11-19. The listed applicant is Bert & Joe'S, Inc.. The 510(k) number is K963955.

When did DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS receive FDA 510(k) clearance?

DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS received FDA 510(k) clearance on 1996-11-19, under 510(k) number K963955.

Who is the listed applicant for DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS?

The FDA 510(k) record lists Bert & Joe'S, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS?

The FDA product code for DR. BERT'S SUNCARE PRODUCTS PEEPER KEEPERS is HQY.

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Related Devices (Code: HQY)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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