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FDA 510(k)

KENWOOD BIOLOGICAL STEOILIZ. INDICATOR

K-Number: K771132 · 1977-07-14

ApplicantWill Ross Co.
Decision Date1977-07-14
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KENWOOD BIOLOGICAL STEOILIZ. INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Will Ross Co.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771132. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENWOOD BIOLOGICAL STEOILIZ. INDICATOR?

KENWOOD BIOLOGICAL STEOILIZ. INDICATOR is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Will Ross Co.. The 510(k) number is K771132.

When did KENWOOD BIOLOGICAL STEOILIZ. INDICATOR receive FDA 510(k) clearance?

KENWOOD BIOLOGICAL STEOILIZ. INDICATOR received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771132.

Who is the listed applicant for KENWOOD BIOLOGICAL STEOILIZ. INDICATOR?

The FDA 510(k) record lists Will Ross Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENWOOD BIOLOGICAL STEOILIZ. INDICATOR?

The FDA product code for KENWOOD BIOLOGICAL STEOILIZ. INDICATOR is FRC.

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Other records listing Will Ross Co. 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.

K780850SEARLE NEONATAL OXYGEN PROBEK771561DOVER URINE METERK770607TRACTION HARNESSK770608WALKING AIDK770609TABLE, MASSAGE & TREATMHNT, FIXED HEIGHTK770611PARALLEL BARS

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Related Devices (Code: FRC)

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.

K260766Celerity 5 HP Biological Indicator (LCB052)STERIS CorporationK252680Celerity™ 20 HP Biological IndicatorSTERIS CorporationK251122Terragene® Bionova® BT20 Biological IndicatorTerrageneK251452Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)SterisK250044Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059); Celerity 20 HP Biological Indicator (LCB044); Celerity 20 HP Challenge Pack (LCB045)STERIS CorporationK250061Celerity IncubatorSTERIS Corporation

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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