SP 4
K-Number: K853541 · 1986-03-28
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ApplicantRobert Bosch Corp.
Decision Date1986-03-28
Product Code
DecisionSubstantially Equivalent for Some Indications
Device Summary
SP 4 is the device name listed in this FDA 510(k) record. The listed applicant is Robert Bosch Corp.. It received FDA 510(k) clearance on 1986-03-28 under 510(k) number K853541. FDA Decision: Substantially Equivalent for Some Indications.
Frequently Asked Questions
What is the SP 4?
SP 4 is a medical device that received FDA 510(k) clearance on 1986-03-28. The listed applicant is Robert Bosch Corp.. The 510(k) number is K853541.
When did SP 4 receive FDA 510(k) clearance?
SP 4 received FDA 510(k) clearance on 1986-03-28, under 510(k) number K853541.
Who is the listed applicant for SP 4?
The FDA 510(k) record lists Robert Bosch Corp. as the applicant. This does not by itself establish the device manufacturer.
Other records listing Robert Bosch 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.
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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