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FDA 510(k)

PROPPER SUPER SERACULT(R)

K-Number: K921798 · 1992-10-05

ApplicantPropper Mfg. Co., Inc.
Decision Date1992-10-05
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PROPPER SUPER SERACULT(R) is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K921798. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPPER SUPER SERACULT(R)?

PROPPER SUPER SERACULT(R) is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K921798.

When did PROPPER SUPER SERACULT(R) receive FDA 510(k) clearance?

PROPPER SUPER SERACULT(R) received FDA 510(k) clearance on 1992-10-05, under 510(k) number K921798.

Who is the listed applicant for PROPPER SUPER SERACULT(R)?

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

What is the FDA product code for PROPPER SUPER SERACULT(R)?

The FDA product code for PROPPER SUPER SERACULT(R) is KHE.

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Other records listing Propper Mfg. Co., Inc. as applicant

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.

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Related Devices (Code: KHE)

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.

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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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