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FDA 510(k)

STRIP, STERILIZATION INDICATOR; DRY HEAT

K-Number: K890761 · 1989-08-07

ApplicantSpsmedical Supply Corp.
Decision Date1989-08-07
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRIP, STERILIZATION INDICATOR; DRY HEAT is the device name listed in this FDA 510(k) record. The listed applicant is Spsmedical Supply Corp.. It received FDA 510(k) clearance on 1989-08-07 under 510(k) number K890761. 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 STRIP, STERILIZATION INDICATOR; DRY HEAT?

STRIP, STERILIZATION INDICATOR; DRY HEAT is a medical device that received FDA 510(k) clearance on 1989-08-07. The listed applicant is Spsmedical Supply Corp.. The 510(k) number is K890761.

When did STRIP, STERILIZATION INDICATOR; DRY HEAT receive FDA 510(k) clearance?

STRIP, STERILIZATION INDICATOR; DRY HEAT received FDA 510(k) clearance on 1989-08-07, under 510(k) number K890761.

Who is the listed applicant for STRIP, STERILIZATION INDICATOR; DRY HEAT?

The FDA 510(k) record lists Spsmedical Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRIP, STERILIZATION INDICATOR; DRY HEAT?

The FDA product code for STRIP, STERILIZATION INDICATOR; DRY HEAT is JOJ.

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Other records listing Spsmedical Supply Corp. as applicant

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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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