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FDA 510(k)

ONCE-A-DAY BOWIE AND DICK TEST PACK.

K-Number: K961156 · 1997-04-01

ApplicantPropper Mfg. Co., Inc.
Decision Date1997-04-01
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ONCE-A-DAY BOWIE AND DICK TEST PACK. 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 1997-04-01 under 510(k) number K961156. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONCE-A-DAY BOWIE AND DICK TEST PACK.?

ONCE-A-DAY BOWIE AND DICK TEST PACK. is a medical device that received FDA 510(k) clearance on 1997-04-01. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K961156.

When did ONCE-A-DAY BOWIE AND DICK TEST PACK. receive FDA 510(k) clearance?

ONCE-A-DAY BOWIE AND DICK TEST PACK. received FDA 510(k) clearance on 1997-04-01, under 510(k) number K961156.

Who is the listed applicant for ONCE-A-DAY BOWIE AND DICK TEST PACK.?

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 ONCE-A-DAY BOWIE AND DICK TEST PACK.?

The FDA product code for ONCE-A-DAY BOWIE AND DICK TEST PACK. is JOJ.

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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.

K111453STEAM DOT BLU PROCESS INDICATORK102894CLASSIX CHEMICAL STERILIZATION INDICATORK082620ONCE-A-DAY VERTOS TEST PACKK031152PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)K991618BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATORK991276PASS/FAIL CHALLENGE PACK

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Related Devices (Code: JOJ)

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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