Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TIME STEAM AUTOCLAVE TAPE

K-Number: K800873 · 1980-05-08

Decision Date1980-05-08
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TIME STEAM AUTOCLAVE TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Professional Tape Co., Inc.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800873. 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 TIME STEAM AUTOCLAVE TAPE?

TIME STEAM AUTOCLAVE TAPE is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Professional Tape Co., Inc.. The 510(k) number is K800873.

When did TIME STEAM AUTOCLAVE TAPE receive FDA 510(k) clearance?

TIME STEAM AUTOCLAVE TAPE received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800873.

Who is the listed applicant for TIME STEAM AUTOCLAVE TAPE?

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

What is the FDA product code for TIME STEAM AUTOCLAVE TAPE?

The FDA product code for TIME STEAM AUTOCLAVE TAPE is JOJ.

Related Clinical Trials

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.

Other records listing Professional Tape 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.

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.

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.

↑