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FDA 510(k)

ACCU. CROWN COLD CURE

K-Number: K771527 · 1977-08-16

ApplicantParker Laboratories, Inc.
Decision Date1977-08-16
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCU. CROWN COLD CURE is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771527. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU. CROWN COLD CURE?

ACCU. CROWN COLD CURE is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K771527.

When did ACCU. CROWN COLD CURE receive FDA 510(k) clearance?

ACCU. CROWN COLD CURE received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771527.

Who is the listed applicant for ACCU. CROWN COLD CURE?

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

What is the FDA product code for ACCU. CROWN COLD CURE?

The FDA product code for ACCU. CROWN COLD CURE is EBG.

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Related Devices (Code: EBG)

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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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