SDC RECTAL TEMP. PROBE PRODUCT #1020
K-Number: K830039 · 1983-02-23
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Device Summary
Frequently Asked Questions
What is the SDC RECTAL TEMP. PROBE PRODUCT #1020?
SDC RECTAL TEMP. PROBE PRODUCT #1020 is a medical device that received FDA 510(k) clearance on 1983-02-23. The listed applicant is Science Development Corp.. The 510(k) number is K830039.
When did SDC RECTAL TEMP. PROBE PRODUCT #1020 receive FDA 510(k) clearance?
SDC RECTAL TEMP. PROBE PRODUCT #1020 received FDA 510(k) clearance on 1983-02-23, under 510(k) number K830039.
Who is the listed applicant for SDC RECTAL TEMP. PROBE PRODUCT #1020?
The FDA 510(k) record lists Science Development Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SDC RECTAL TEMP. PROBE PRODUCT #1020?
The FDA product code for SDC RECTAL TEMP. PROBE PRODUCT #1020 is FLL.
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 Science Development Corp. 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: FLL)
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.
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