SDC ORAL-RECTAL TEMP. PROBE
K-Number: K832392 · 1983-09-12
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Device Summary
Frequently Asked Questions
What is the SDC ORAL-RECTAL TEMP. PROBE?
SDC ORAL-RECTAL TEMP. PROBE is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Science Development Corp.. The 510(k) number is K832392.
When did SDC ORAL-RECTAL TEMP. PROBE receive FDA 510(k) clearance?
SDC ORAL-RECTAL TEMP. PROBE received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832392.
Who is the listed applicant for SDC ORAL-RECTAL TEMP. PROBE?
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 ORAL-RECTAL TEMP. PROBE?
The FDA product code for SDC ORAL-RECTAL TEMP. PROBE 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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